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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]
The molecular formula C 4 H 7 BrO 2 (molar mass: 167.002 g/mol, ... 2-Bromobutyric acid; Ethyl bromoacetate This page was last edited on 13 February 2021, at 02: ...
The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu. 1-Fluorobutane can be obtained by reacting 1-bromobutane with potassium fluoride in ethylene glycol .
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 NaO 3: sodium oxybate (C 4 H 7 NO) n: Poly(N-vinylacetamide) Poly(N-vinylacetamide) C 4 H 7 NO 2: 1-Aminocyclopropanecarboxylic acid: 22059-21-8 C 4 H 7 NO 3: aceturic acid: C 4 H 7 ...
Butyric acid (/ ˈ b j uː t ɪ r ɪ k /; from Ancient Greek: βούτῡρον, meaning "butter"), also known under the systematic name butanoic acid, is a straight-chain alkyl carboxylic acid with the chemical formula CH 3 CH 2 CH 2 COOH. It is an oily, colorless liquid with an unpleasant odor. Isobutyric acid (2-methylpropanoic acid) is an ...
A buffer solution is a solution where the pH does not change significantly on dilution or if an acid or base is added at constant temperature. [1] Its pH changes very little when a small amount of strong acid or base is added to it. Buffer solutions are used as a means of keeping pH at a nearly constant value in a wide variety of chemical ...
Molar concentration or molarity is most commonly expressed in units of moles of solute per litre of solution. [1] For use in broader applications, it is defined as amount of substance of solute per unit volume of solution, or per unit volume available to the species, represented by lowercase : [2]
For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix "cyclo alkyl -" (e.g. "cyclohexyl-") or for benzene, "phenyl-".