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2-Bromobutyric acid is the organic compound with the molecular formula CH 3 CH 2 CH(Br)CO 2 H. It is a colorless liquid. The 2-position is stereogenic, so the compound is chiral. Optical resolution can be effected using strychnine. [1]
2-Bromobutyric acid; Ethyl bromoacetate This page was last edited on 13 February 2021, at 02:16 (UTC). Text is available under the Creative Commons Attribution ...
8-Hydroxycarbostyril 1 is acylated with 2-bromobutyric acid chloride 2 at the fifth position of the quinoline system, which gives the compound 3. This undergoes action of isopropylamine, forming an aminoketone, the carbonyl group of which is reduced by sodium borohydride, giving procaterol 4 .
C. Calconcarboxylic acid; Candesartan; Candoxatril; Canrenoic acid; Captopril; Carbenzide; Carbestrol; Carbonic acid; Carboxyatractyloside; 9-Carboxymethoxymethylguanine
2-bromobutyric acid: 80-58-0 4-bromobutyric acid: 2623-87-2 α-bromoisobutyric acid: 2052-01-9 ethyl bromoacetate: 105-36-2 C 4 H 7 KO 3: potassium oxybate: C 4 H 7 ...
Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene. These conditions lead to the anti-Markovnikov addition, i.e. give the 1-bromo derivatives. [2] 1-Bromobutane can also be prepared from butanol by treatment with hydrobromic acid: [3] CH 3 (CH 2) 3 OH + HBr → CH 3 (CH 2) 3 Br + H 2 O
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Crotonic acid ((2E)-but-2-enoic acid) is a short-chain unsaturated carboxylic acid described by the formula CH 3 CH=CHCO 2 H. The name crotonic acid was given because it was erroneously thought to be a saponification product of croton oil. [2] It crystallizes as colorless needles from hot water. With a cis-alkene, Isocrotonic acid is an isomer ...