CAS 62214-39-5
:(S)-3-butene-1,2-diol
Description:
(S)-3-butene-1,2-diol, with the CAS number 62214-39-5, is an organic compound characterized by its structure, which includes a butene backbone with hydroxyl (-OH) groups at the first and second carbon positions. This compound is a chiral molecule, existing in two enantiomeric forms, with the (S)-configuration being one of them. It is a colorless to pale yellow liquid at room temperature and is soluble in water due to the presence of hydroxyl groups, which can form hydrogen bonds. The compound exhibits properties typical of alcohols, including the ability to participate in various chemical reactions such as oxidation and esterification. Its reactivity can be influenced by the double bond present in the butene structure, making it a potential intermediate in organic synthesis. Additionally, (S)-3-butene-1,2-diol may have applications in pharmaceuticals, agrochemicals, and as a building block in the synthesis of more complex organic molecules. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C4H8O2
InChI:InChI=1/C4H8O2/c1-2-4(6)3-5/h2,4-6H,1,3H2/t4-/m0/s1
SMILES:C=C[C@@H](CO)O
Synonyms:- (2S)-but-3-ene-1,2-diol
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Found 3 products.
(S)-3-Butene-1,2-diol
CAS:(S)-3-Butene-1,2-diol is a catalytic chiral molecule that is used in asymmetric synthesis. It has been shown to be effective in the synthesis of epoxides and carboxylic acids. The enzyme catalytic enantioselective activity was discovered by the use of trichloroacetonitrile as an enantiomeric substrate. It can also be used to synthesize chiral dna adducts and prochiral profiles. This molecule has been found to be carcinogenic and should not be handled without protection.Formula:C4H8O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:88.11 g/mol
