Ziarno, Malgorzata et al. published their research in Zywnosc in 2004 | CAS: 5743-47-5

Calcium 2-hydroxypropanoate pentahydrate (cas: 5743-47-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Reference of 5743-47-5

Impact of calcium salts addition on stability of milk used in cottage cheese production was written by Ziarno, Malgorzata;Semeniuk, Ewa;Kycia, Katarzyna. And the article was included in Zywnosc in 2004.Reference of 5743-47-5 This article mentions the following:

An effective way to increase Ca levels in cottage cheese is the addition of Ca salts to the pasteurized processed milk prior to its heat treatment (repasteurization). The impact of different Ca salts (Ca L-lactate pentahydrate, Ca lactogluconate dihydrate, Ca gluconate, CaCl2, Ca citrate tetrahydrate, CaCO3) added on the heat stability and some physicochem. properties of the processed milk used to manufacture cottage cheese was examined The water-soluble Ca salts (L-lactate, lactogluconate, gluconate, CaCl2) added to the milk increased its acidity. The Ca-fortified milk had decreased heat stability and milk proteins precipitated during milk repasteurization (74°C for 5 min). The highest quantity of a water-soluble Ca salt added that did not precipitate the proteins during repasteurization was the addition of 0.15% anhydrous CaCl2; with this addition the Ca content in the processed milk was increased by 55 mg%. An addnl. test for heat stability of milk proteins indicated that it was better to add 35 mg% Ca as CaCl2 or 20 mg% Ca as the other Ca salts. The addition of water-insoluble Ca salts (citrate, carbonate) allowed to increase the Ca levels in the processed milk without neg. effects of protein precipitation Addition of even 5% of these Ca salts caused no decrease in the protein heat stability and no coagulation during the milk repasteurization. Various Ca salt combinations added to the processed milk provided higher Ca levels compared with single Ca salts added. When 63 mg% Ca as citrate and 20 mg% Ca as lactate were added together, the Ca level rose by 83 mg%. The use of Ca salt mixtures did not precipitate the proteins. In the experiment, the researchers used many compounds, for example, Calcium 2-hydroxypropanoate pentahydrate (cas: 5743-47-5Reference of 5743-47-5).

Calcium 2-hydroxypropanoate pentahydrate (cas: 5743-47-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Reference of 5743-47-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kuang, Haifeng et al. published their research in Journal of Polymer Research in 2020 | CAS: 109-17-1

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Safety of ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate)

Using facile one-pot thiol-ene reaction to prepare elastomers filled with silica was written by Kuang, Haifeng;Yin, Qiyan;Zhang, Ruyi;Wang, Penghan;Gou, Kai;Chen, Huan;Dai, Chenghao;Weng, Gengsheng. And the article was included in Journal of Polymer Research in 2020.Safety of ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) This article mentions the following:

Novel elastomers filled with different contents of silica through a two-step one-pot thiol-ene reaction were reported. Two monomers of poly (ethylene glycol) dimethacrylate and 1,6-hexanedithiol were used in the first step to synthesize a vinyl-terminated prepolymer at room temperature In the second step, silica and chem. cross-linker trimethylolpropane tris(3-mercaptopropionate) were directly added to the prepolymer in sequence and transparent elastomers were obtained in 30 min at room temperature The crosslinking kinetics and mech. properties in the presence of different contents of silica were investigated in detail by rheol., tensile and cyclic loading measurements. It was found that silica had a significant reinforcing effect on the mech. properties of the elastomers. Our synthetic method is simple, solvent-free and energy- and cost-efficient. Our findings pave a new way to fabricate novel sulfur-containing elastomers using thiol-ene chem. In the experiment, the researchers used many compounds, for example, ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1Safety of ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate)).

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Safety of ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate)

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kangas, L. et al. published their research in Hormone and Metabolic Research in 2014 | CAS: 128607-22-7

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Application of 128607-22-7

Effects of Ospemifene on Breast Tissue Morphology and Proliferation: A Comparative Study Versus Other Selective Estrogen Receptor Modulators in Ovariectomized Rats was written by Kangas, L.;Harkonen, P.;Vaananen, K.;Keskitalo, J.;Eigeliene, N.. And the article was included in Hormone and Metabolic Research in 2014.Application of 128607-22-7 This article mentions the following:

Ospemifene is a tissue-selective estrogen agonist/antagonist that was recently approved for the treatment of dyspareunia associated with vulvar and vaginal atrophy, which occurs in up to approx. 50% of postmenopausal women. The current analyses were conducted to determine whether ospemifene exhibits estrogenic activity in the mammary glands of ovariectomized rats and to compare potential estrogenic activity with selective estrogen receptor modulators (tamoxifen, raloxifene, and toremifene). Three sep. studies with differing durations (6, 9, and 28 days) were conducted using similar procedures in ovariectomized Sprague-Dawley rats. Estradiol treatment and sham-treated ovariectomized rats were used as pos. and neg. controls, resp. Cell proliferation was examined using labeled 5-bromo-2-deoxyuridine; cytoplasmic prolactin was characterized with antibody staining. The morphol. of the mammary gland was studied by histol. staining of sections from the right fourth mammary glands, and the excised gland from the left side was used for counting the lobulus number Neither ospemifene nor selective estrogen receptor modulators substantially induced 5-bromo-2-deoxyuridine staining, altered the morphol. of the mammary glands, or changed prolactin immunostaining in ovariectomized rats compared with the ovariectomized controls. With the exception of toremifene, the selective estrogen receptor modulators did not cause a substantial induction in mammary gland lobuli. Estradiol had effects opposite to those of the selective estrogen receptor modulators in these studies. Ospemifene exhibited no substantial estrogenic activity in the mammary gland of ovariectomized rats. Activity in the mammary gland of ovariectomized rats with ospemifene was comparable to raloxifene and tamoxifen. In the experiment, the researchers used many compounds, for example, (Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7Application of 128607-22-7).

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Application of 128607-22-7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Addonizio, M. L. et al. published their research in Journal of Alloys and Compounds in 2015 | CAS: 109-17-1

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Formula: C16H26O7

Preparation method of double-textured ZnO:B films deposited by MOCVD on plasma etched polymer buffer was written by Addonizio, M. L.;Fusco, L.. And the article was included in Journal of Alloys and Compounds in 2015.Formula: C16H26O7 This article mentions the following:

With the aim of enhancing light trapping phenomenon in PV thin film silicon devices, a method was developed to produce highly textured TCO surfaces by the growth of ZnO:B on a buffer layer consisting of UV-cured highly transparent acrylic polymer (IBA) whose surface had been modified by RIE process. Different RIE etching conditions, particularly RF-power and process duration, were used to obtain different polymer surface modifications. The effect of different treatment conditions on polymer surface was systematically studied and subsequently correlated to the properties of ZnO:B films deposited by MOCVD on these modified polymer surfaces. The surface morphol. of zinc oxide film, growth on IBA buffer layer, changed from conventional pyramid-like single-texture to cauliflower-like double-texture. The morphol. of double-textured ZnO strongly depended on the surface properties of the etched polymer. Excellent scattering properties were obtained and at the wavelength of 800 nm the haze value increased from 7.5% (pyramidal-like single-texture ZnO layer on glass) to 68% (double textured ZnO film obtained on etched IBA, treated for 20 min at RF-power of 80 W). The root-mean-square roughness showed similar behavior: it increased at the increasing of the etching time and the highest value of 160 nm was obtained for cauliflower-like ZnO:B film. Good elec. properties were maintained for double-textured ZnO:B films with excellent scattering properties. In the experiment, the researchers used many compounds, for example, ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1Formula: C16H26O7).

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Formula: C16H26O7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Soldati, Chiara et al. published their research in EMBO Molecular Medicine in 2021 | CAS: 128607-22-7

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Computed Properties of C24H23ClO2

Repurposing of tamoxifen ameliorates CLN3 and CLN7 disease phenotype was written by Soldati, Chiara;Lopez-Fabuel, Irene;Wanderlingh, Luca G.;Garcia-Macia, Marina;Monfregola, Jlenia;Esposito, Alessandra;Napolitano, Gennaro;Guevara-Ferrer, Marta;Scotto Rosato, Anna;Krogsaeter, Einar K.;Paquet, Dominik;Grimm, Christian M.;Montefusco, Sandro;Braulke, Thomas;Storch, Stephan;Mole, Sara E.;De Matteis, Maria A.;Ballabio, Andrea;Sampaio, Julio L.;McKay, Tristan;Johannes, Ludger;Bolanos, Juan P.;Medina, Diego L.. And the article was included in EMBO Molecular Medicine in 2021.Computed Properties of C24H23ClO2 This article mentions the following:

Batten diseases (BDs) are a group of lysosomal storage disorders characterized by seizure, visual loss, and cognitive and motor deterioration. We discovered increased levels of globotriaosylceramide (Gb3) in cellular and murine models of CLN3 and CLN7 diseases and used fluorescent-conjugated bacterial toxins to label Gb3 to develop a cell-based high content imaging (HCI) screening assay for the repurposing of FDA-approved compounds able to reduce this accumulation within BD cells. We found that tamoxifen reduced the lysosomal accumulation of Gb3 in CLN3 and CLN7 cell models, including neuronal progenitor cells (NPCs) from CLN7 patient-derived induced pluripotent stem cells (iPSC). Here, tamoxifen exerts its action through a mechanism that involves activation of the transcription factor EB (TFEB), a master gene of lysosomal function and autophagy. In vivo administration of tamoxifen to the CLN7δex2 mouse model reduced the accumulation of Gb3 and SCMAS, decreased neuroinflammation, and improved motor coordination. These data strongly suggest that tamoxifen may be a suitable drug to treat some types of Batten disease. In the experiment, the researchers used many compounds, for example, (Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7Computed Properties of C24H23ClO2).

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Computed Properties of C24H23ClO2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Alzari, Valeria et al. published their research in Polymer in 2014 | CAS: 109-17-1

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Related Products of 109-17-1

Three component terpolymer and IPN hydrogels with response to stimuli was written by Alzari, Valeria;Ruiu, Andrea;Nuvoli, Daniele;Sanna, Roberta;Martinez, Javier Illescas;Appelhans, Dietmar;Voit, Brigitte;Zschoche, Stefan;Mariani, Alberto. And the article was included in Polymer in 2014.Related Products of 109-17-1 This article mentions the following:

Two different types of multi-stimuli-shrinking hydrogels were synthesized (IPNs and terpolymeric hydrogels) by properly polymerizing N-isopropylacrylamide, 2-hydroxyethyl methacrylate and 2-acrylamido-2-methylpropanesulfonic acid in various mutual ratios and different synthetic orders. Both classical (CP) and frontal (FP) polymerizations were used and the resulting material properties compared. The best compositions and synthetic routes were found and the swelling, morphol. and thermal material properties were studied. The results show that some IPNs exhibit marked stimuli-shrinking properties while some terpolymers present an opposite behavior. IPNs swell more than terpolymers and show a sharper stimuli-response, with a larger swelling ratio variation. In addition, FP allowed obtaining samples with the same characteristic of CP materials, but with significant preparation advantages. It has been demonstrated that by varying monomer mutual ratio, synthetic technique (FP or CP) and structural architecture (terpolymers or IPNs), different materials having peculiar properties and characteristics can be obtained. In the experiment, the researchers used many compounds, for example, ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1Related Products of 109-17-1).

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Related Products of 109-17-1

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Koskimies, Pasi et al. published their research in International Journal of Clinical Pharmacology and Therapeutics in 2013 | CAS: 128607-22-7

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.HPLC of Formula: 128607-22-7

Oral bioavailability of ospemifene improves with food intake was written by Koskimies, Pasi;Katila, Kirsi;Lammintausta, Risto;Aaltonen, Anne-Mari;Vuorinen, Jouni;Saarni, Outi;Scheinin, Mika. And the article was included in International Journal of Clinical Pharmacology and Therapeutics in 2013.HPLC of Formula: 128607-22-7 This article mentions the following:

Objective: To assess the effect of concomitant food intake on the relative bioavailability of ospemifene and its main metabolite, 4-hydroxyospemifene, after single oral dosing. Methods: This was an open-label, randomized, balanced, two-treatment (fed vs. fasted), two-period, two-sequence cross-over study in 24 healthy male subjects. Single 60-mg doses of ospemifene were administered without food or with a high-fat, high-energy breakfast (860 kcal). In an extension study, a single 60-mg dose of ospemifene was given to 12 subjects with a low-fat, light breakfast (300 kcal). Addnl. information was acquired by determining tablet dissolution profiles in media which reflected fasted and fed intestinal conditions. Results: The AUC0-72h and Cmax of ospemifene were 2.8- and 3.6-fold higher after a high-fat breakfast and 1.9- and 2.3-fold higher after a low-fat breakfast when compared with an overnight fast. The variability in both primary pharmacokinetic parameters was considerably reduced (by up to 50%) with a meal, indicating more consistent absorption of ospemifene with concomitant food intake. Dissolution in conditions simulating fed intestinal fluid (high bile acid concentration) was increased 3-fold compared with dissolution in simulated fasted intestinal fluid. Conclusions: Food markedly enhanced the extent and predictability of ospemifene absorption. The increase in bioavailability was not linearly related with the fat content of the meal. In vitro dissolution results were consistent with these clin. observations. Administration with food enhances and standardizes the oral bioavailability of ospemifene. Thus, it is recommended that ospemifene tablets should be taken with food. In the experiment, the researchers used many compounds, for example, (Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7HPLC of Formula: 128607-22-7).

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.HPLC of Formula: 128607-22-7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Schiavi, Michele Carlo et al. published their research in Gynecological Endocrinology in 2017 | CAS: 128607-22-7

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 128607-22-7

Retrospective analysis in 46 women with vulvovaginal atrophy treated with ospemifene for 12 weeks: improvement in overactive bladder symptoms was written by Schiavi, Michele Carlo;Zullo, Marzio Angelo;Faiano, Pierangelo;D’Oria, Ottavia;Prata, Giovanni;Colagiovanni, Vanessa;Giannini, Andrea;Di Tucci, Chiara;Perniola, Giorgia;Di Donato, Violante;Monti, Marco;Muzii, Ludovico;Benedetti Panici, Pierluigi. And the article was included in Gynecological Endocrinology in 2017.HPLC of Formula: 128607-22-7 This article mentions the following:

Aims: The aim of this study was to assess the effectiveness and safety of ospemifene in the improvement of overactive bladder (OAB) symptoms in postmenopausal women affected by vulvovaginal atrophy (VVA). Methods: Forty-six postmenopausal patients affected by VVA with OAB syndrome were enrolled for the study. All patients received Ospemifene 60 mg for 12 wk. Clin. examination, 3-day voiding diary, urodynamic testing, ultrasound measurement of endometrial and bladder wall thickness (BWT) and the Vaginal Health Index (VHI) were performed at baseline and 12 wk. Patients completed the OAB-Q SF and UDI-6. Results: After 12-wk, the number of patients with detrusor overactivity decreased from 39% to 13% (p = 0.04). The reduction in the mean number in 24 h of voids (9.57 ± 2.12 vs. 6.63 ± 1.22, p < 0.0001), urgent micturition episodes/24 h (5.63 ± 1.46 vs. 1.44 ± 1.31, p < 0.0001), nocturia episodes (3.17 ± 0.85 vs. 1.11 ± 1.18, p < 0.0001), urinary incontinence episodes/24 h (0.85 ± 0.96 vs. 0.33 ± 0.64, p = 0.003) was observed The UDI-6, OAB-Q symptoms, OAB-Q (HRQL) scores were 8.95 ± 0.91 vs. 5.56 ± 1.40, 62.60 ± 14.70 vs. 20.08 ± 10.83 and 18.71 ± 7.41 vs. 79.45 ± 14.47 (p < 0.001) before and after 12 wk. Conclusion: Ospemifene is an effective potential therapy for postmenopausal women with VVA improving OAB symptoms and quality of life. In the experiment, the researchers used many compounds, for example, (Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7HPLC of Formula: 128607-22-7).

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 128607-22-7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Bansal, Sumit et al. published their research in Journal of Pharmacology and Experimental Therapeutics in 2019 | CAS: 128607-22-7

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Reference of 128607-22-7

Inhibition of human sulfotransferase 2A1-catalyzed sulfonation of lithocholic acid, glycolithocholic acid, and taurolithocholic acid by selective estrogen receptor modulators and various analogs and metabolites was written by Bansal, Sumit;Lau, Aik Jiang. And the article was included in Journal of Pharmacology and Experimental Therapeutics in 2019.Reference of 128607-22-7 This article mentions the following:

The present study was done to characterize the sulfonation of LCA, GLCA, and TLCA and to investigate whether triphenylethylene (clomifene, tamoxifen, toremifene, ospemifene, droloxifene), benzothiophene (raloxifene, arzoxifene), tetrahydronaphthalene (lasofoxifene, nafoxidine), indole (bazedoxifene), and benzopyran (acolbifene) classes of selective estrogen receptor modulator (SERM) inhibit LCA, GLCA, and TLCA sulfonation. Human recombinant SULT2A1, but not SULT2B1b or SULT1E1, catalyzed LCA, GLCA, and TLCA sulfonation, whereas each of these enzymes catalyzed DHEA sulfonation. LCA, GLCA, and TLCA sulfonation is catalyzed by human liver cytosol, and SULT2A1 followed the substrate inhibition model with comparable apparent Km values (=1 muM). The potency and extent of inhibition of LCA sulfonation were attenuated or increased by structural modifications to toremifene, bazedoxifene, and lasofoxifene. The inhibitory effect of raloxifene, bazedoxifene, and acolbifene on LCA sulfonation was also observed in HepG2 human hepatocellular carcinoma cells. Overall, among the SERMs investigated, bazedoxifene and raloxifene were the most effective inhibitors of LCA, GLCA, and TLCA sulfonation. These findings provide insight into the structural features of specific SERMs that contribute to their inhibition of SULT2A1-catalyzed LCA sulfonation. Inhibition of LCA, GLCA, and TLCA detoxification by a SERM may provide a biochem. basis for adverse effects associated with a SERM. In the experiment, the researchers used many compounds, for example, (Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7Reference of 128607-22-7).

(Z)-2-(4-(4-Chloro-1,2-diphenylbut-1-en-1-yl)phenoxy)ethan-1-ol (cas: 128607-22-7) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Reference of 128607-22-7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Garcia, Hermano et al. published their research in Annals of Medicine (Abingdon, United Kingdom) in 2021 | CAS: 109-17-1

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Synthetic Route of C16H26O7

Restorative materials without Bis-GMA – myth or reality was written by Garcia, Hermano;Fernandes, Ines Caldeira;Caldeira, Jorge;Pinto, Alexandra;Carpinteiro, Ines;Azul, Ana. And the article was included in Annals of Medicine (Abingdon, United Kingdom) in 2021.Synthetic Route of C16H26O7 This article mentions the following:

IntroductionThe Bis-GMA, which is known to possess toxic properties to the human body, is part of the chem. structure of several direct dental restorative materials [1]. However, currently, there are composite resins on the market that are free of this monomer [2]. From the dental resin are released many other compounds [3]. The aim of this study was to analyze the composition of restorative materials from three different brands, and to verify whether or not Bis-GMA monomers are present in their composition Materials and methodsSamples of the Enamel plus HRi Universal Dentin (Micerium), Enamel plus HRi Bio Function (Micerium), Filtek One Bulk Fill Restorative (3 M ESPE) and Admira Fusion (VOCO) resins were prepared using three different methods: light-curing resin specimens placed for 18 min in an ethanol/water solution; light-curing resin specimens placed for 180 min in an ethanol/water solution; resin samples eluted in an acetonitrile solution without being photopolymerized These samples were analyzed using the HPLC (High Performance Liquid Chromatog.) technique.ResultsHEMA, Bis-GMA and UDMA monomers were found in the composite resin Enamel plus HRi Universal Dentin (Micerium); UDMA monomers were detected in Enamel plus HRi Bio Function (Micerium); UDMA and TEGDMA monomers were revealed in Filtek One Bulk Fill Restorative (3 M ESPE), and HEMA and UDMA peaks were obtained in Admira Fusion (VOCO). Discussion and conclusionsThe release of most of the residual monomers occurs in the first minutes after polymerization As shown in the results, the difference of the concentrations of monomers, detected by the HPLC method, between the resins eluted during 18 min and 180 min, was not significant. It was concluded that in samples of non-polymerized resins, it is possible to detect a larger number of residual monomers, and that Bis-GMA is only present in Enamel plus HRi Universal Dentin (Micerium) resin. In the experiment, the researchers used many compounds, for example, ((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1Synthetic Route of C16H26O7).

((Oxybis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl) bis(2-methylacrylate) (cas: 109-17-1) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Synthetic Route of C16H26O7

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts