CAS 20697-04-5
:2-(3-Chlorophenyl)oxirane
Description:
2-(3-Chlorophenyl)oxirane, also known as a chlorinated epoxide, is an organic compound characterized by its epoxide functional group, which consists of a three-membered cyclic ether. The presence of the 3-chlorophenyl group indicates that a chlorine atom is substituted on the aromatic ring, influencing the compound's reactivity and physical properties. This compound typically exhibits a relatively low boiling point and is likely to be a colorless to pale yellow liquid at room temperature. Its structure allows for potential electrophilic reactions, making it useful in various synthetic applications, particularly in the production of pharmaceuticals and agrochemicals. The chlorine substituent can enhance the compound's biological activity and lipophilicity, affecting its interaction with biological systems. As with many epoxides, 2-(3-Chlorophenyl)oxirane may pose health risks, including skin and respiratory irritation, and should be handled with appropriate safety precautions in a controlled laboratory environment.
Formula:C8H7ClO
InChI:InChI=1S/C8H7ClO/c9-7-3-1-2-6(4-7)8-5-10-8/h1-4,8H,5H2
InChI key:InChIKey=YVMKRPGFBQGEBF-UHFFFAOYSA-N
SMILES:ClC=1C=C(C=CC1)C2CO2
Synonyms:- (2R)-2-(3-chlorophenyl)oxirane
- (3-Chlorophenyl)oxirane
- (R)-(+)-(3-Chlorophenyl)oxirane
- (m-Chlorophenyl)oxirane
- 2-(3-Chlorophenyl)oxirane
- 3-Chloroepoxystyrene
- 3-Chlorostyrene Oxide
- 3-Fluorophenyl ethylene oxide
- Benzene, 1-chloro-3-(epoxyethyl)-
- Oxirane, (3-chlorophenyl)-
- Oxirane, 2-(3-chlorophenyl)-
- See more synonyms
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Found 3 products.
2-(3-Chloro-phenyl)-oxirane
CAS:Formula:C8H7ClOPurity:97.0%Color and Shape:LiquidMolecular weight:154.592-(3-Chloro-phenyl)-oxirane
CAS:<p>2-(3-Chloro-phenyl)-oxirane is a reactive molecule with the chemical formula C6H4ClO2. It is an epoxide that can be obtained by ring-opening of acetone cyanohydrin. 2-(3-Chloro-phenyl)-oxirane has been used as a glycosidic bond in the synthesis of α-amino acid derivatives and as a substrate for ring opening polymerization. This compound is also used to study the mechanism of enantioselective reactions, such as kinetic and thermodynamic studies, which can lead to the development of new methods for producing enantiopure compounds.<br>2-(3-Chloro-phenyl)-oxirane has been shown to inhibit growth in E. coli K12 and S. typhimurium at concentrations between 10 and 100 μM; it also inhibits growth in ovary cells at concentrations between 5 and 50 μM. The inhibition of bacterial</p>Formula:C8H7ClOPurity:Min. 95%Molecular weight:154.6 g/mol


