Tag: 100-200

New intermediates for the paint and coatings industries was written by Petersen, Leslie. And the article was included in Kemia – Kemi in 1996.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Neste Oxo, a part of Neste’s chems. division, serves the paint and surface coatings industry with a range of products. The Nexcoat family of coating intermediates are targeted at the fast-growing market for polyester-based coating. Nexcoat 600 (neopentyl glycol) is used in saturated polyesters for powder coating and polyester-based binders. Nexcoat 700 (2-butyl-2-ethyl-1,3-propanediol) serves some of the same markets but provides improved properties, including higher solubility in hydrocarbons, lower viscosity, lower water absorption, excellent hydrolytic stability, and improved flexibility. 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. 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 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Partial molar volumes of organic solutes in water. XXV. Branched aliphatic diols at temperatures (298 to 573) K and pressures up to 30 MPa was written by Cibulka, Ivan. And the article was included in Journal of Chemical Thermodynamics in 2014.Product Details of 115-84-4 The following contents are mentioned in the article:

Densities of dilute aqueous solutions of three branched diols derived from propane-1,3-diol (2-methyl-2-propylpropane-1,3-diol, 2,2-diethylpropane-1,3-diol, and 2-ethyl-2-butylpropane-1,3-diol) and of 3-methylpentane-1,5-diol measured over the temperature range from (298 to 573) K and at pressures up to 30 MPa using a flow vibrating-tube densimeter are reported. Standard molar volumes were evaluated from the measured data. Present data were combined with those obtained previously for related solutes and relations to the structures of solute mols. are discussed. Predictions of standard molar volumes based on group contribution approach were tested and analyzed. 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. 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.Product Details of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tests with repellents against the American dog tick was written by Cole, M. M.;Lloyd, Geo. W.. And the article was included in Journal of Economic Entomology in 1955.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Di-Bu adipate (I) repelled 86% of Dermacentor variablis when applied at the rate of 2 g. per sq. ft. of trouser cloth. Percentage repellence of mixts of equal parts of 2-butyl-2-ethyl-1,3-propanediol (II), benzyl benzoate (III), and N-butylacetanilide (IV) was 93%, equal parts of II, III, and IV with 1% lindane 89% equal parts of I, II, and IV 86%, equal parts of N-butyl-4-cyclohexene-1,2-dicarboximide (V), undecenoic acid (VI) and IV 83%, equal parts of II, III, and N-propylacetanilide 76%, equal parts of II, IV, and VI 75%, equal parts of I, II, and III 73%, equal parts of II, IV, and V 72%, and equal parts of II, III, and N-isopropylacetanilide 65%. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Ultraviolet and infrared spectrophotometric analysis of an insect-repellent mixture was written by Sassaman, Warren A.;Cohen, S. P.. And the article was included in Applied Spectroscopy in 1954.Computed Properties of C9H20O2 The following contents are mentioned in the article:

A spectrophotometric procedure employing measurements in both the ultraviolet and infrared regions was developed to determine the concentrations of N-butylacetanilide, benzyl benzoate, 2-ethyl-2-butyl-1,3-propanediol, and Tween 80, in a mixture containing only these 4 components. The first 2 components have relatively strong absorptivities in the ultraviolet at 227.5 and 280.3 millimicrons, while the latter 2 have absorption bands at the infrared wave lengths, 8.99 and 9.60 microns. By substituting the absorptivities at these wave lengths in a set of 4 simultaneous equations, the percentage of each component in an insect-repellent mixture is calculated This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Computed Properties of C9H20O2).

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. 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.Computed Properties of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Corn earworm moth repellents was written by Roberts, James E.;Rolston, L. H.. And the article was included in J. Kansas Entomol. Soc. in 1958.Related Products of 115-84-4 The following contents are mentioned in the article:

The following materials tested in cages exhibited significant repellency against corn earworm moth oviposition: N-butylacetanilide, dimethyl phthalate, 2-butyl-2-ethyl-1,3-propanediol, Tat (75% dimethyl phthalate and 25% dimethylbicycloheptenedicarboxylate), and undecenoic acid. Little or no repellency was exhibited by N-ethylacetanilide, dibutyl adipate, benzyl benzoate, hexyl benzoate, caprylic acid, diphenyl carvonate, cinnamic acid, 2-phenylcyclohexanol, 2,3,4,5-bis (Δ²-butenylene) tetrahydrofurfural, butoxypolypropylene glycol, 2-ethyl-1,3-hexanediol, dibutyl phthalate, isobornyl thiocyanoacetate, and N,N-diethyl-m-toluamide. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Related Products of 115-84-4).

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. 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.Related Products of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthetic ester lubricants was written by Barnes, R. S.;Fainman, M. Z.. And the article was included in Lubrication Engineering in 1957.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Phys. properties and coefficients of friction were determined for esters of neopentyl glycol, tri(hydroxymethyl)ethane, tri(hydroxymethyl)propane, pentaerythritol, 2-butyl-2-ethyl-1,3-propanediol, and 2,2,4-trimethyl-1,3-pentanediol with n-C₉, n-C₁₀, n-C₁₄ and n-C₁₈ acids from natural sources, highly branched acids obtained by the Oxo process, and mixed normal and branched acids obtained by caustic extraction of the liquid product from CO hydrogenation. Study of the thermal decomposition at 260° of selected esters indicated that its rate is generally greatly increased by H in the β position. 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. 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Safety of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Recyclable cobalt(0) nanoparticle catalysts for hydrogenations was written by Bueschelberger, Philipp;Reyes-Rodriguez, Efrain;Schoettle, Christian;Treptow, Jens;Feldmann, Claus;Jacobi von Wangelin, Axel;Wolf, Robert. And the article was included in Catalysis Science & Technology in 2018.SDS of cas: 106-21-8 The following contents are mentioned in the article:

The search for new hydrogenation catalysts that replace noble metals is largely driven by sustainability concerns and the distinct mechanistic features of 3d transition metals. Several combinations of cobalt precursors and specific ligands in the presence of reductants or under high-thermal conditions were reported to provide active hydrogenation catalysts. This study reports a new method of preparation of small, monodisperse Co(0) nanoparticles (3-4 nm) from the reduction of com. CoCl₂ in the absence of ligands or surfactants. High catalytic activity was observed in hydrogenations of alkenes, alkynes, imines, and heteroarenes (2-20 bar H₂). The magnetic properties enabled catalyst separation and multiple recyclings. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8SDS of cas: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.SDS of cas: 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Non-thermal microwave effects in radical polymerization of bio-based terpenoid (meth)acrylates was written by Castagnet, Thibault;Agirre, Amaia;Ballard, Nicholas;Billon, Laurent;Asua, Jose M.. And the article was included in Polymer Chemistry in 2020.Application In Synthesis of 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

Microwave-assisted polymerization represents an opportunity to develop efficient polymerization strategies for the synthesis of (bio)macromols. with improved properties. The possibilities will increase tremendously if non-thermal microwave effects, i.e. effect of microwaves on the kinetic constants, are operative, because we can increase at the same time conversion and mol. weight This work investigates these effects in the free radical polymerization of bio-based terpenoid (meth)acrylates finding that terpenoid acrylates present a strong non-thermal microwave effect, whereas the methacrylate ones do not show any effect. The reasons for these findings are discussed and the results compared with the apparently conflicting literature. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Application In Synthesis of 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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.Application In Synthesis of 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Molecular docking study, synthesis and evaluation of antitumor activity of novel pyrazole derivatives was written by Jebastin, J. Nelson Samuel;Kumar, T. Ramesh;Evangelin, D.. And the article was included in International Journal of Pharmaceutical and Chemical Sciences in 2016.HPLC of Formula: 52010-89-6 The following contents are mentioned in the article:

A series of (benzylideneamino)phenyl-1H-pyrazol-3(2H)-one derivatives I [R = 3-Me, 3,6-(OH)₂, 2,4,6-(NH₂)₃, etc.] was synthesized via condensation of 4-aminoantipyrine with benzaldehydes. All the synthesized compounds were evaluated for for their ability to inhibit cell proliferation in cancer cell lines and tested in silico for their interaction with histone deacetylase (HDAC8) enzyme. Based on the docking score, compound I [R = 3-Br-6-OH] showed highest docking score of -6.4061, which is important for HDAC8 inhibition. Among the synthesized compounds, compound I [R = 3-Br-6-OH] showed promising activity against human cervical cancer cell line. This study involved multiple reactions and reactants, such as 2,5-Dihydroxy-4-methylbenzaldehyde (cas: 52010-89-6HPLC of Formula: 52010-89-6).

2,5-Dihydroxy-4-methylbenzaldehyde (cas: 52010-89-6) 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.HPLC of Formula: 52010-89-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Desymmetrization of Diols by Phosphorylation with a Titanium-BINOLate Catalyst was written by Ouellette, Erik T.;Lougee, Marshall G.;Bucknam, Andrea R.;Endres, Paul J.;Kim, John Y.;Lynch, Emma J.;Sisko, Elizabeth J.;Sculimbrene, Bianca R.. And the article was included in Journal of Organic Chemistry in 2021.COA of Formula: C9H20O2 The following contents are mentioned in the article:

The desymmetrization of ten prochiral diols by phosphoryl transfer with a titanium-BINOLate complex is discussed. The phosphorylation of nine 1,3-propane diols is achieved in yields of 50-98%. Enantiomeric ratios as high as 92:8 are achieved with diols containing a quaternary C-2 center incorporating a protected amine. The chiral ligand, base, solvent, and stoichiometry are evaluated along with a nonlinear effect study to support an active catalyst species that is oligomeric in chiral ligand. The use of pyrophosphates as the phosphorylating agent in the desymmetrization facilitates a user-friendly method for enantioselective phosphorylation with desirable protecting groups (benzyl, o-nitrobenzyl) on the phosphate product. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4COA of Formula: C9H20O2).

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.COA of Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts