Bains, Amreen K.’s team published research in Catalysis Science & Technology in 2020 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Electric Literature of C7H7BrO It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde.

《Mechanistic insight into the azo radical-promoted dehydrogenation of heteroarene towards N-heterocycles》 was written by Bains, Amreen K.; Adhikari, Debashis. Electric Literature of C7H7BrOThis research focused ontriazine pyrimidine preparation mechanism kinetics; alc amidine hydrochloride dehydrogenation nickel catalyst. The article conveys some information:

Herein, a molecularly defined nickel catalyst, which can perform two annulation reactions under mild conditions (80°, 8 h), towards the sustainable synthesis of triazine I (R = H, 4-Me, 4-F, etc.) and pyrimidine II (R = H, 4-Me, 2-F, etc.; R1 = Me, C6H5, 4-MeC6H4, 4-FC6H4) has been reported. Mechanistically, the important role of the catalyst in promoting the dehydrogenation of heteroarenes is clearly described. The binding of the saturated heterocycle to the metal catalyst underwent a pre-equilibrium step (K = 238 at 80°), which is followed by a crucial hydrogen atom transfer. A series of kinetics experiments including Van’t Hoff, Eyring anal. and interception of pyrimidinyl radical disclosed the details of the dehydrogenation process. This ligand-driven, base metal catalytic approach is significantly different from the considerably evaluated metal-ligand cooperative bond activation strategies, which may offer an alternative dehydrogenation pathway that demands less energy.(4-Bromophenyl)methanol(cas: 873-75-6Electric Literature of C7H7BrO) was used in this study.

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Electric Literature of C7H7BrO It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Hosseini, Saber’s team published research in Photochemistry and Photobiology in 2019 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Electric Literature of C7H7BrO It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

《Nano-WO3-SO3H as a New Photocatalyst Insight Through Covalently Grafted Bronsted Acid: Highly Efficient Selective Oxidation of Benzyl Alcohols to Aldehydes》 was written by Hosseini, Saber; Amoozadeh, Ali; Akbarzadeh, Yasaman. Electric Literature of C7H7BrOThis research focused ontungsten oxide benzyl alc aldehyde Bronsted acid oxidation. The article conveys some information:

Modification of nano-WO3 with -SO3H groups as a covalently grafted solid acid reduced its band-gap energy from 2.8 to 2.4 eV and made it an ideal nominee for photocatalytic reaction under visible light irradiation This nano-photocatalyst has been successfully used for the selective oxidation of different benzyl alcs. to corresponding aldehydes under blue LED irradiation The reaction became approx. two times faster with excellent yields. It has shown that the nitrobenzene as an available industrial oxidant is applicable for photocatalytic oxidation of benzyl alc.; remarkably high yield and selectivity have been observed The experimental process involved the reaction of (4-Bromophenyl)methanol(cas: 873-75-6Electric Literature of C7H7BrO)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Electric Literature of C7H7BrO It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Shah, Sk. Sheriff’s team published research in Chemistry – A European Journal in 2020 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.COA of Formula: C7H7BrO It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde.

《Organophotoredox-Mediated Amide Synthesis by Coupling Alcohol and Amine through Aerobic Oxidation of Alcohol》 was published in Chemistry – A European Journal in 2020. These research results belong to Shah, Sk. Sheriff; Shee, Maniklal; Venkatesh, Yarra; Singh, Amit Kumar; Samanta, Samya; Singh, N. D. Pradeep. COA of Formula: C7H7BrO The article mentions the following:

The combination of an organic photocatalyst [4CzIPN (1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene) or 5MeOCzBN (2,3,4,5,6-pentakis(3,6-dimethoxy-9 H-carbazol-9-yl)benzonitrile)], quinuclidine, and tetra-n-butylammonium phosphate (hydrogen-bonding catalyst) was employed for amide bond formations. The hydrogen-bonded OH group activated the adjacent C-H bond of alcs. towards hydrogen atom transfer (HAT) by a radical species. The quinuclidinium radical cation, generated through single-electron oxidation of quinuclidine by the photocatalyst, employed to abstract a hydrogen atom from the α-C-H bond of alcs. selectively due to a polarity effect-produced α-hydroxyalkyl radical, which subsequently converted to the corresponding aldehyde under aerobic conditions. Then the coupling of the aldehyde and an amine formed a hemiaminal intermediate that upon photocatalytic oxidation produced the amide. In the part of experimental materials, we found many familiar compounds, such as (4-Bromophenyl)methanol(cas: 873-75-6COA of Formula: C7H7BrO)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.COA of Formula: C7H7BrO It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zhang, Meng-Juan’s team published research in Organic & Biomolecular Chemistry in 2019 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.SDS of cas: 873-75-6 It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.

The author of 《Reaction condition controlled nickel(II)-catalyzed C-C cross-coupling of alcohols》 were Zhang, Meng-Juan; Li, Hong-Xi; Young, David J.; Li, Hai-Yan; Lang, Jian-Ping. And the article was published in Organic & Biomolecular Chemistry in 2019. SDS of cas: 873-75-6 The author mentioned the following in the article:

A controlled approach to a diverse range of β-alkylated secondary alcs., α-alkylated ketones and α,β-unsaturated ketones using the acceptorless dehydrogenation coupling methodol. employing a Ni(II) 4,6-dimethylpyrimidine-2-thiolate cluster catalyst under different reaction conditions was reported. This catalyst could tolerate a wide range of substrates and exhibited a high activity for the annulation reaction of secondary alcs. with 2-aminobenzyl alcs. to yield quinolines. This work is an example of precise chemoselectivity control by careful choice of reaction conditions. In the part of experimental materials, we found many familiar compounds, such as (4-Bromophenyl)methanol(cas: 873-75-6SDS of cas: 873-75-6)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.SDS of cas: 873-75-6 It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Hosseini, Seyed Mohammad’s team published research in New Journal of Chemistry in 2021 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Formula: C7H7BrO It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde.

Hosseini, Seyed Mohammad; Karimi, Meghdad; Safarifard, Vahid published an article in 2021. The article was titled 《Metal-organic framework/carbon nitride nanosheets composites (TMU-49/CNNSs): efficient photocatalyst for aerobic oxidation of alcohols under visible light》, and you may find the article in New Journal of Chemistry.Formula: C7H7BrO The information in the text is summarized as follows:

Oxidation reactions are considered as a challenging issue at the industrial scale. As several traditional methods are not biocompatible and safe, there is a need to develop sustainable photocatalytic approaches that employ mol. oxygen as the terminal oxidant. Herein, a cobalt-based metal-organic framework (MOF) was hybridized with graphitic carbon nitride nanosheets (CNNSs), namely TMU-49/CNNSs, using a facile in situ ultrasound-assisted synthesis, for the catalytic photo-oxidation of benzyl alc. under visible light irradiation The oxidation was carried out with variation of four parameters: solvent, catalyst amount, time and light source. Characterization of as-prepared samples was performed by Fourier-transform IR spectroscopy, thermogravimetric anal., X-ray powder diffraction, N2 adsorption-desorption, SEM, and UV-visible diffuse reflection spectra. The TMU-49/CNNSs composite exhibited remarkable photocatalytic activity under visible light irradiation; the oxidation yield reached almost 80% for benzyl alc. after 3 h reaction. The superior photocatalytic activity of the MOF/CNNSs composite is attributed to enhanced separation of the photogenerated electron-hole pairs and increased visible-light absorption. After reading the article, we found that the author used (4-Bromophenyl)methanol(cas: 873-75-6Formula: C7H7BrO)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Formula: C7H7BrO It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Xia, Qiangqiang’s team published research in Asian Journal of Organic Chemistry in 2019 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Formula: C7H7BrO It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.

In 2019,Asian Journal of Organic Chemistry included an article by Xia, Qiangqiang; Shi, Zuodong; Yuan, Jiangpei; Bian, Qilong; Xu, Yuanqing; Liu, Baoying; Huang, Yongwei; Yang, Xiaobo; Xu, Hao. Formula: C7H7BrO. The article was titled 《Visible-light-enabled selective oxidation of primary alcohols through hydrogen-atom transfer and its application in the synthesis of quinazolinones》. The information in the text is summarized as follows:

A visible-light-enabled selective oxidation of alcs. to aldehydes RCHO [R = (CH2)4CH3, Ph, 2-thienyl, etc.] was developed under transition-metal-free conditions. Utilizing eosin Y as the direct hydrogen-atom transfer (HAT) photocatalyst and mol. oxygen as the terminal oxidant, both aromatic and aliphatic aldehydes could be obtained in moderate to good yields. Using this approach, various quinazolinones I [R1 = Me, Ph, 4-BrC6H4, etc.; R2 = H, Cl, Br, MeO, NO2; R3 = H, n-Pr, n-hexyl, etc.], including two real drug mols., were easily synthesized from the corresponding o-aminobenzamides and alcs. In the part of experimental materials, we found many familiar compounds, such as (4-Bromophenyl)methanol(cas: 873-75-6Formula: C7H7BrO)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Formula: C7H7BrO It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Cantillo, R.’s team published research in Journal of Physics: Conference Series in 2019 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Quality Control of (4-Bromophenyl)methanol It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

In 2019,Journal of Physics: Conference Series included an article by Cantillo, R.; Percino, J.; Murillo, E. A.. Quality Control of (4-Bromophenyl)methanol. The article was titled 《Synthesis and characterization of a derivative of carbazole obtained from bromobenzyl alcohol》. The information in the text is summarized as follows:

4-(9H-Carbazol-9-yl)benzenemethanol has been prepared by the reaction of carbazole and 4-bromobenzyl alc. The compound has been characterized by X-ray diffraction, IR and UV-visible spectroscopies, and 1H NMR. Its thermal stability has been evaluated. 4-(9H-Carbazol-9-yl)benzenemethanol exhibits yellow fluorescence. In the part of experimental materials, we found many familiar compounds, such as (4-Bromophenyl)methanol(cas: 873-75-6Quality Control of (4-Bromophenyl)methanol)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Quality Control of (4-Bromophenyl)methanol It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Das, Vivek’s team published research in European Journal of Inorganic Chemistry in 2019 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Recommanded Product: (4-Bromophenyl)methanol It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

The author of 《A Self-Assembled Heterometallic {Co7-Ho1} Nanocluster: 3d-4f Trimeric Keggin-Type Silicotungstate [HoCo7Si3W29O108(OH)5 (H2O)4]18- and its Catalytic and Magnetic Applications》 were Das, Vivek; Khan, Imran; Hussain, Firasat; Sadakane, Masahiro; Hageo, Kazuki; Ichihashi, Katsuya; Inoue, Katsuya; Nishihara, Sadafumi. And the article was published in European Journal of Inorganic Chemistry in 2019. Recommanded Product: (4-Bromophenyl)methanol The author mentioned the following in the article:

A new self assembled Co2+ and Ho3+-substituted polyoxometalate have been synthesized using a trilacunary Keggin-type silicotungstate. The polyanion complex of the formula [HoCo7Si3W29O108(OH)5(H2O)4]18- (1) has a trimeric crystal structure which displayed an excellent catalytic and magnetic property. Here, the authors have carried out selective oxidation of various alc. substrates such as derivatives of benzyl alc., cyclohexanol etc. to its corresponding aldehydes/ketones. The paramagnetic nature of the compound was seen from the magnetic study. However, antiferromagnetic interaction was observed between Co2+-Co2+ or Co2+-Ho3+ at a very low temperature The compound was characterized by FTIR, UV/Visible spectroscopy, Single crystal x-ray diffraction, X-ray powder diffraction, high-resolution electrospray ionization mass spectroscopy (HR-ESI-MS) and TGA. The experimental part of the paper was very detailed, including the reaction process of (4-Bromophenyl)methanol(cas: 873-75-6Recommanded Product: (4-Bromophenyl)methanol)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Recommanded Product: (4-Bromophenyl)methanol It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Adil, Syed Farooq’s team published research in Applied Organometallic Chemistry in 2020 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Synthetic Route of C7H7BrO It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

《Efficient aerial oxidation of different types of alcohols using ZnO nanoparticle-MnCO3-graphene oxide composites》 was published in Applied Organometallic Chemistry in 2020. These research results belong to Adil, Syed Farooq; Assal, Mohamed E.; Shaik, Mohammed Rafi; Kuniyil, Mufsir; Hashmi, Azhar; Khan, Mujeeb; Khan, Aslam; Tahir, Muhammad Nawaz; Al-Warthan, Abdulrahman; Siddiqui, Mohammed Rafiq H.. Synthetic Route of C7H7BrO The article mentions the following:

In this study, nanocomposites of graphene oxide (GRO) and ZnO nanoparticle-doped MnCO3 ([ZnO-MnCO3/(1%)GRO]) were synthesized via a facile, straightforward co-precipitation technique. Interestingly, it was noticed that the incorporation of GRO in the catalytic system could noticeably improve the catalytic efficiency compared to a catalyst (ZnO-MnCO3) without GRO, for aerial oxidation of benzyl alc. (BzOH) employing O2 as a nature-friendly oxidant under base-free conditions. The impacts of various reaction factors were thoroughly explored to optimize reaction conditions using oxidation of BzOH to benzaldehyde (BzH) as a model substrate. The catalysts were characterized using X-ray diffraction, thermogravimetric anal., Fourier transform IR spectroscopy, field-emission SEM, Energy dispersive X-ray spectroscopy (EDX), Brunauer-Emmett-Teller (BET), and Raman spectroscopy. The (1%)ZnO-MnCO3/(1%)GRO exhibited significant specific activity (67 mmol.g-1.hr-1) with full conversion of BzOH and >99% BzH selectivity within just 6 min. The catalytic efficiency of the (1%)ZnO-MnCO3/(1%)GRO nanocomposite was significantly better than the (1%)ZnO-MnCO3/(1%)HRG and (1%)ZnO-MnCO3 catalysts, presumably due to the existence of oxygen-possessing groups on the GRO surface and as well as a very high surface area that could have been instrumental in uniformly dispersing the active sites of the catalyst, i.e., ZnO-MnCO3. Under optimum circumstances, various kinds of alcs. ROH (R = benzyl, furan-2-ylmethyl, cyclohexyl, 1-phenylethyl, etc.) were selectively transformed to resp. carbonyls, e.g., cyclohexanone with full convertibility over the (1%)ZnO-MnCO3/(1%)GRO catalyst. Furthermore, the highly effective (1%)ZnO-MnCO3/(1%)GRO catalyst could be successfully reused and recycled over five consecutive runs with a marginal reduction in its performance and selectivity.(4-Bromophenyl)methanol(cas: 873-75-6Synthetic Route of C7H7BrO) was used in this study.

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Synthetic Route of C7H7BrO It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Sabaghi, Maryam’s team published research in Journal of Organometallic Chemistry in 2020 | CAS: 873-75-6

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Computed Properties of C7H7BrO It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

《Fabrication of a new heterogeneous tungstate-based on the amino-functionalized metal-organic framework as an efficient catalyst towards sonochemical oxidation of alcohols under green condition》 was written by Sabaghi, Maryam; Aghajani, Zahra; Najafi, Gholam Reza. Computed Properties of C7H7BrOThis research focused ontungstate amino functionalized metal organic framework catalyst preparation; aldehyde ketone preparation green chem ultrasound irradiation; alc sonochem oxidation. The article conveys some information:

Ultrasonic-assisted reactions, as a green technique, are often more efficient compared to those traditional protocols. To this end, the selective and solvent-free oxidation of aromatic alcs. to the corresponding aldehydes and ketones were investigated in the presence of Co-ABDC/W at room temperature under ultrasonic irradiation conditions for the first time in this paper. The structure, particle size, thermal stability, and morphol. of the fabricated heterogeneous catalyst and the products were characterized by FT-IR, EDS, FE-SEM, XRD, TGA, and GC analyses. In this regard, immobilization of tungstate had a significant effect on thermal stability (around 450° for 40% weight loss) and catalytic performance. Moreover, the efficiency of two different oxidation methods, including ultrasound irradiations and reflux, were comparatively investigated by GC spectrometry. Obtained sonoxidn. results presented higher conversions ranging (84 to 100%) than reflux condition via shorter reaction times. The influences of the reaction parameters, such as hydrogen peroxide concentration, and catalyst loading, were also investigated. The proposed method offers several advantages, such as excellent conversions, selective oxidations, environmentally-benign procedure, short reaction times, and easy workup. Notably, this is the first report that focuses on using amino-functionalized MOFs with ultrasonic irradiation for selective oxidation reactions. The experimental part of the paper was very detailed, including the reaction process of (4-Bromophenyl)methanol(cas: 873-75-6Computed Properties of C7H7BrO)

(4-Bromophenyl)methanol(cas: 873-75-6) undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls.Computed Properties of C7H7BrO It is used in the synthesis of amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts