Category: 115-84-4

A convenient biphasic process for the monosilylation of symmetrical 1,n-primary diols was written by Yu, Chengzhi;Liu, Bin;Hu, Longqin. And the article was included in Tetrahedron Letters in 2000.SDS of cas: 115-84-4 The following contents are mentioned in the article:

A simple and mild biphasic process was developed for the selective protection of one of two chem. equivalent primary hydroxyl groups in 1,n-diols using t-butyldiphenyl silyl chloride in diisopropyl Et amine (DIEA) and DMF. E.g., a solution of 2-Butyl-2-ethylpropanediol in DMF (3 mL) was charged with DIEA (10 equiv), to which mixture was added TBDPSCl (1.05 equiv) with stirring to give the corresponding monosilylated product in 92% yield. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4SDS of cas: 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. 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.SDS of cas: 115-84-4

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Direct formation of oxetanes by pyrolysis of diprimary diols in the presence of catalysts was written by Jaubert, Michele;Mazet, Michel;Yvernault, Theophile. And the article was included in Bulletin de la Societe Chimique de France in 1974.Application of 115-84-4 The following contents are mentioned in the article:

Oxetanes I (R = Et, Pr, Bu, CHMe2, H, Me; R1 = H, Me, Et, Pr, Bu, CHMe2, CMe3, CHPrMe, CHPrEt, (CH2)4Me) were prepared in ≤24% yield by pyrolyzing RR1C(CH2OH)2, the acetals II, or the formals III in the presence of pumice at 350°. A pumice-diol ratio of 5 gave the highest yields. The yields of I also increased with the size of R and R1. Pyrolysis of I (R = R1 = Et) gave Et2CHCHO, Et2C:CH2, EtPrCHCHO, EtMeCHCOEt, PrMeCHCOMe. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application of 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. 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.Application of 115-84-4

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

A comparison of different herbicides applied at planting, emergence, and post-emergence on field corn was written by Marshall, E. R.;Loeffler, G.. And the article was included in Proceedings of the Northeastern Weed Control Conference in 1954.Product Details of 115-84-4 The following contents are mentioned in the article:

The low volatile esters of 2,4-D, Sinox PE (alkanolamine salt of dinitro-ο-sec-butylphenol), Crag Herbicide I (2,4-dichlorophenoxy Et sulfate), and Bu ester of MCP were most effective when applied at the time of emergence of the field corn. Amino triazole and Dalapon (CH₃CCl₂COOH) gave grass control but caused injury to the corn when used as directional sprays in post-emergence applications. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Product Details of 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. 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.Product Details of 115-84-4

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Alcohol – Wikipedia,
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Use of 2-butyl-2-ethyl-1,3-propanediol in polyester resins for coil coatings was written by Vaahtio, Marja. And the article was included in European Coatings Journal in 1998.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

A report on the phys. properties of polyester resins and coatings containing different amounts of 2-butyl-2-ethyl-1,3-propanediol and 1,6-hexanediol is given. Topics include the synthesis of the resins, phys. properties of the resins (e.g. glass transition temperature, hydroxyl values) and the coatings (e.g. viscosity, flexibility vs. hardness, weathering, stain and MEK-rub resistance), and a brief discussion of the exptl. obtained results. Moreover, the effect of addnl. adipic acid, for enhanced flexibility, on the coating properties was determined This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Safety of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. 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.Safety of 2-Butyl-2-ethylpropane-1,3-diol

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Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kinetics in the AA/TMPD and AA/BEPD reaction system was written by Zhang, Wei-lu;Zhang, Dong;Zhao, Ya-juan. And the article was included in Changchun Gongye Daxue Xuebao, Ziran Kexueban in 2006.Formula: C9H20O2 The following contents are mentioned in the article:

The removal of the byproduct, water, during polyesterification process between diacids and diols may have some effects on the kinetics parameters. Concerning the effects, kinetics parameters in AA/BEPD and AA/TMPD systems, such as rate constant-k’, activation energy-E’ and re-exponential factor-A’ are calculated Then they are compared with the one which neglects the effects. Results show that the relative errors between the two will increase when the temperature raise. Especially in the high temperature, the error may increase to 12%. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Formula: C9H20O2).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. 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.Formula: C9H20O2

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Alcohol – Wikipedia,
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Influence of molecular structure on transparency of powder coating in synthesis of polyester was written by Pan, Cong-yi;Liu, Liang;Luo, Qing;Wang, Wei-yue;Li, Yong. And the article was included in Xiandai Tuliao Yu Tuzhuang in 2017.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

From the perspective of the raw materials of synthetic polyester resin, curing agent, leveling agent and so on were added to the resin synthesized by different monomers. After melt-extrusion, blending, grinding and sieving, spray it on the glass mirror plate to detect the impact of different synthetic monomer on transparency of coating film. At the same time, the acid value, crystallinity and other indicators of polyester resins were also tested to determine their impact on the transparency of polyester powder coating. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Category: alcohols-buliding-blocks).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

3,7-Dioxaazelaamides as ionophores for lithium ion selective liquid membrane electrodes was written by Metzger, Erich;Aeschimann, Roland;Egli, Martin;Suter, Gaby;Dohner, Rene;Ammann, Daniel;Dobler, Max;Simon, Wilhelm. And the article was included in Helvetica Chimica Acta in 1986.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

Neutral lipophilic dioxaazelaamides I (R = H, Me, CMe₂; R¹ = H, Me, Et; R² = H, Me, Bu) were prepared and incorporated in lipophilic liquid membranes. Li⁺-Na⁺ selectivities of these were ≤80; the membranes allow reliable measurements of Li⁺ in blood serum within the clin. concentration range. The structure of the LiSCN complex with I (R = H; R¹ = R² = Me) was determined by x-ray crystallog. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Category: alcohols-buliding-blocks).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Recovery of boric acid from wastewater by solvent extraction was written by Matsumoto, Michiaki;Kondo, Kazuo;Hirata, Makoto;Kokubu, Shuzo;Hano, Tadashi;Takada, Tokio. And the article was included in Separation Science and Technology in 1997.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

An extraction system for the recovery of boric acid using 2-butyl-2-ethyl-1,3-propanediol (BEPD) as an extractant was studied. Loss of the extractant to the aqueous solution was lowered by using 2-ethylhexanol as a diluent. The extraction equilibrium of boric acid with BEPD was clarified, and the equilibrium constants for various diluents were determined Furthermore, continuous operation for the recovery of boric acid using mixer-settlers for extraction and stripping was successfully conducted for 100 h. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Category: alcohols-buliding-blocks).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Category: alcohols-buliding-blocks

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Alcohol – Wikipedia,
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Anticonvulsant activity of carbamate esters of certain 2,2-disubstituted 1,3-propanediols was written by Berger, F. M.. And the article was included in Journal of Pharmacology and Experimental Therapeutics in 1952.Reference of 115-84-4 The following contents are mentioned in the article:

cf. C.A. 45, 265a; 46, 1651d. The intensity and duration of the anticonvulsant action against electroshock seizures in mice were determined for the 2,2-disubstituted dimethyl, methylethyl, methylisopropyl, diethyl, ethylbutyl, ethylphenyl, dipropyl, and diphenyl derivatives of 1,3-propanediol. The diols and their monocarbamates were short-acting and weak. The dicarbamates showed a longer and stronger anticonvulsant action. The cyclic carbonate esters, which may also be called 5,5-disubstituted 1,3-dioxan-2-one derivatives, showed a weak and transient anticonvulsant action. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Reference of 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Reference of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

2-Substituted 1,3-propanediols as extractants of boric acid was written by Bernane, A.;Svarcs, E.;Timoteus, H.;Hansens, T.. And the article was included in Latvijas PSR Zinatnu Akademijas Vestis, Kimijas Serija in 1987.Product Details of 115-84-4 The following contents are mentioned in the article:

The distribution of H₃BO₃ in the organic and aqueous phases in extraction by diisobutyl-1,3-propanediol, 2-octyl-1,3-propanediol, 2-ethyl-2-butyl-1,3-propanediol, and 1-(3-bromophenyl)-2,2-dimethyl-1,3-propanediol was studied. The effects of diluents (HCCl₃, PhMe, acetophenone, isoamyl alc., C₂Cl₄, decyl alc.) and salting out agents (NaCl, KCl, MgSO₄, MgCl₂) in H₃BO₃ extraction were determined The extraction effectiveness of the substituted propanediols was closely similar. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Product Details of 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) 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. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Product Details of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts