Tag: 100-200

Control of the pine root color weevil was written by Finnegan, R. J.;Stewart, K. E.. And the article was included in Journal of Economic Entomology in 1962.Safety of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Ethylene dichloride was effective in killing the larvae of Hylobius radicis, but failed to prevent reinfestation. Lindane and dieldrin applied as water emulsions directly to the ground around the base of the trees effectively controlled the insect for at least 4 years. 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. 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.Safety of 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Transformations of diols and cyclic ethers. XXXI. Dehydration of 1,3-diols on metal catalysts was written by Bartok, Mihaly;Molnar, Arpad. And the article was included in Acta Chimica Academiae Scientiarum Hungaricae in 1973.Formula: C9H20O2 The following contents are mentioned in the article:

It has been exptl. confirmed that the transformation of the diols with the accompanying formation of oxo compounds can be observed not only on the vicinal diols but, with a change in the exptl. conditions, on certain types of 1,3-diols too. 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. 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.Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

A general asymmetric synthesis of phenylglycinols was written by Pan, Xingang;Jia, Liangbin;Liu, Xuejian;Ma, Haikuo;Yang, Wenqian;Schwarz, Jacob B.. And the article was included in Tetrahedron: Asymmetry in 2011.SDS of cas: 496856-52-1 The following contents are mentioned in the article:

Hydride reduction and deprotection of siloxymethyl sulfinimines, e.g., I, reliably furnished chiral phenylglycinols, e.g., II or III, in high overall yield and enantiomeric purity. This study involved multiple reactions and reactants, such as (S)-2-Amino-2-(3-chloro-4-fluorophenyl)ethanol (cas: 496856-52-1SDS of cas: 496856-52-1).

(S)-2-Amino-2-(3-chloro-4-fluorophenyl)ethanol (cas: 496856-52-1) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 496856-52-1

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthesis of ester oils was written by Asinger, Friedrich;Fell, Bernhard;Pfeifer, Josef;Iqbal, Abul F. M.. And the article was included in Erdoel & Kohle, Erdgas, Petrochemie in 1970.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

Viscosity and pour point data were reported for esters made from trimethyladipic acid or 1,10-decanedioic acid with various polyfunctional or monofunctional alcs. The latter included hydrogenation products from Versatic Acid 911. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Name: 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. 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.Name: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Organic treatment of titanium dioxide pigments was written by Luginsland, Hans Hermann. And the article was included in FATIPEC Congress in 1987.COA of Formula: C9H20O2 The following contents are mentioned in the article:

The use of neopentyl glycols, trimethylolalkanes, and amino glycols to improve the dispersibility of TiO₂ and the brightness of paints containing the pigments was discussed. 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. 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.COA of Formula: C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Gas chromatography of insect repellents was written by Acree, Fred Jr.;Beroza, C. Morton. And the article was included in Journal of Economic Entomology in 1962.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

Thirteen insect repellents (aromatic amides, esters, and branched chain diols) were separated on either Carbowax 20 M, Silicone 550, or Tide. A column of 15% Carbowax 20 M on acid-washed Columpak at a temperature of 246° was most satisfactory. Approx. 0.2 mg. of each repellent was sufficient for an analysis in an instrument using a thermal conductivity detector and a recorder having a 2.5-my. full span. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4HPLC of Formula: 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. 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.HPLC of Formula: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Study on boiling water resistance of polyester resin for TGIC powder coating was written by Luo, Yi;Xie, Jing;Li, Yong;Liu, Liang;Shi, Yuan-tang;Chen, Li. And the article was included in Xiandai Tuliao Yu Tuzhuang in 2017.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:

The effect of different amount of 2-butyl-2-ethyl-1,3-propanediol (BEPD), isophthalic acid (PIA) and additives on the boiling water resistance, mech. behavior of powder coatings were discussed. The boiling water resistance was analyzed with contact angle and scanning electron microscope. The results showed that the increasing BEPD and PIA was helpful to improve the water boiling resistance performance. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol).

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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Recommanded Product: 2-Butyl-2-ethylpropane-1,3-diol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Publication was written by Anonymous. And the article was included in Research Disclosure in 1999.Recommanded Product: 115-84-4 The following contents are mentioned in the article:

Environmental concerns have resulted in reduced sulfur content in diesel fuels. As a consequence of hydrotreating processes also the amount of lubricating compounds has decreased. Poor lubricity can lead to wear problems especially in rotary pumps. The wear can be prevented by providing lubricity additives in the fuel. Reformulated diesel fuel of the winter grade characteristics was used in this study. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Recommanded Product: 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.Recommanded Product: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Silver-catalyzed remote Csp³-H functionalization of aliphatic alcohols was written by Zhu, Yuchao;Huang, Kaimeng;Pan, Jun;Qiu, Xu;Luo, Xiao;Qin, Qixue;Wei, Jialiang;Wen, Xiaojin;Zhang, Lizhi;Jiao, Ning. And the article was included in Nature Communications in 2018.HPLC of Formula: 106-21-8 The following contents are mentioned in the article:

Herein, a silver-catalyzed δ-selective Csp³-H bond functionalization of abundant and inexpensive aliphatic alcs is reported. Valuable oximonitrile substituted alcs. I (R = Et, n-Bu, Bn, etc.) are easily obtained by using well-designed sulfonyl reagents under simple and mild conditions. This protocol realizes the challenging δ-selective C-C bond formation of simple alkanols. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8HPLC of Formula: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) 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. 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.HPLC of Formula: 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Rh(III)-Catalyzed three-component C-H functionalization reaction with vinylene carbonate: Late-stage C-H esterification of indole derivatives was written by Li, Bin-Shi;Guo, Huai-Xuan;Sun, Wei;Sun, Meng. And the article was included in Tetrahedron Letters in 2022.Name: 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

An efficient and robust Rh(III)-catalyzed three-component C-H esterification reaction of indole derivatives with vinylene carbonate to access indolyl acetates was developed. This protocol exhibited high efficiency, good yields and excellent functional group tolerance. Significantly, this method provided a powerful approach for the late-stage modification of indole-based substrates and natural alcs. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Name: 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. 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.Name: 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts