CAS 141394-10-7
:(S)-2-(2-Chlorophenyl)oxirane
Description:
(S)-2-(2-Chlorophenyl)oxirane, also known as a chiral epoxide, is a chemical compound characterized by its three-membered cyclic ether structure, which includes an oxygen atom and two carbon atoms. The presence of the 2-chlorophenyl group contributes to its unique reactivity and potential applications in organic synthesis. This compound is typically colorless to pale yellow and may exhibit a distinct odor. Its chirality, indicated by the (S) configuration, suggests that it can exist as enantiomers, which may have different biological activities. The epoxide functional group is known for its ability to undergo ring-opening reactions, making it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. Additionally, (S)-2-(2-Chlorophenyl)oxirane may exhibit specific interactions with biological systems, which can be explored for potential therapeutic applications. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, this compound is of interest in both synthetic chemistry and medicinal chemistry due to its structural features and reactivity.
Formula:C8H7ClO
Synonyms:- (2S)-2-(2-chlorophenyl)oxirane
- Oxirane, 2-(2-chlorophenyl)-, (2S)-
- (S)-2-(2-Chlorophenyl)oxirane
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Found 3 products.
(S)-2-(2-Chlorophenyl)oxirane
CAS:Controlled ProductFormula:C8H7ClOColor and Shape:NeatMolecular weight:154.594(2S)-2-(2-Chlorophenyl)oxirane
CAS:<p>(2S)-2-(2-Chlorophenyl)oxirane is an aromatic hydrocarbon that is used to make organic chemicals. It is a racemate and can be used as an enantioselective epoxide hydrolase substrate, which has been shown to have microbial activity. The enzyme catalyzes the formation of an epoxide from (2S)-2-(2-chlorophenyl)oxirane. This reaction can be performed with high enantioselectivity and in low yields for the synthesis of chiral epoxides.</p>Formula:C8H7ClOPurity:Min. 95%Molecular weight:154.59 g/mol
