Detail of > 62600-71-9
- CAS Number:
- 62600-71-9
- Name:
Oxirane,2-(3-chlorophenyl)-, (2R)-
- Superlist Name:
- (R)-3-Chlorostyrene oxide
- Formula:
- C8H7ClO
- Molecular Structure:

- Synonyms:
- Oxirane,(3-chlorophenyl)-, (2R)- (9CI);Oxirane, (3-chlorophenyl)-, (R)-;(2R)-2-(3-Chlorophenyl)oxirane;(R)-(3-Chlorophenyl)oxirane;(R)-2-(3-Chlorophenyl)oxirane;(R)-3-Chlorostyrene epoxide;(R)-3-Chlorostyreneoxide;(R)-m-Chlorostyrene oxide;
- Molecular Weight:
- 154.59
- Density:
- 1.283 g/cm3
- Boiling Point:
- 229.4 °C at 760 mmHg
- Flash Point:
- 97.6 °C
- Hazard Symbols:
Xi- Risk Codes:
- 36/37/38-43
- Safety:
- 26-36/37Details
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Reference
- Process for the preparation of optically active 2-halo-1-(substituted phenyl) ethanol
- Process for the preparation of optically active 2-halo-1-(substituted phenyl) ethanol. Tanaka, Ken; Yasuda, Mari; Ueda, Makoto (Mitsubishi Chemical Corporation, Japan). Eur. Pat. Appl. EP 792936 A2 3 Sep 1997, 18 pp. DESIGNATED STATES: R: CH, DE, FR, GB, IT, LI. 62600-71-9 are also occured in this study. 62600-71-9 are also occured in this study. (English). (European Patent Organization). CODEN: EPXXDW. CLASS: ICM: C12P041-00. ICS: C12P007-22; C07D303-02. APPLICATION: EP 1997-103346 28 Feb 1997. PRIORITY: JP 1996-41441 28 Feb 1996. DOCUMENT TYPE: Patent CA Section: 16 (Fermentation and Bioindustrial Chemistry) The present invention provides an industrially advantageous process for the prepn. of an optically active 2-halo-1-(substituted phenyl)ethanol useful as medicines, agricultural chems., or as intermediates thereof and a simple process for the prepn. of an optically active substituted styrene oxide or 2-amino-1-(substituted phenyl)ethanol useful as medicines, agricultural chems. or intermediates thereof. A 2-halo-1-(substituted phenyl)ethanol represented by the following general formula (I) is allowed to contact, in the presence of a carboxylic anhydride, with an enzyme stereoselectively catalyzing ester interchange to produce an optically active 2-halo-1-(substituted phenyl)ethanol of formula I (wherein X represents a Cl or Br atom and R1, R2, and R3 may be the same or different and each represents H, a halogen atom, a C1-5 alkyl group, a C1-5 haloalkyl group, a C1-5 alkoxy group, a CN group, or a NO2 group, with the proviso that when 2 of R1, R2 and R3 are alkyl groups or alkoxy groups, they may be combined together to form a ring and that all of R1, R2, and R3 are not H atoms at the same time). ..
- Process for the preparation of optically active 2-halo-1-(substituted phenyl) ethanol
- Process for the preparation of optically active 2-halo-1-(substituted phenyl) ethanol. Tanaka, Ken; Yasuda, Mari; Ueda, Makoto (Mitsubishi Chemical Corporation, Japan). Eur. Pat. Appl. EP 792936 A2 3 Sep 1997, 18 pp. DESIGNATED STATES: R: CH, DE, FR, GB, IT, LI. 62600-71-9 are also occured in this study. 62600-71-9 are also occured in this study. (English). (European Patent Organization). CODEN: EPXXDW. CLASS: ICM: C12P041-00. ICS: C12P007-22; C07D303-02. APPLICATION: EP 1997-103346 28 Feb 1997. PRIORITY: JP 1996-41441 28 Feb 1996. DOCUMENT TYPE: Patent CA Section: 16 (Fermentation and Bioindustrial Chemistry) The present invention provides an industrially advantageous process for the prepn. of an optically active 2-halo-1-(substituted phenyl)ethanol useful as medicines, agricultural chems., or as intermediates thereof and a simple process for the prepn. of an optically active substituted styrene oxide or 2-amino-1-(substituted phenyl)ethanol useful as medicines, agricultural chems. or intermediates thereof. A 2-halo-1-(substituted phenyl)ethanol represented by the following general formula (I) is allowed to contact, in the presence of a carboxylic anhydride, with an enzyme stereoselectively catalyzing ester interchange to produce an optically active 2-halo-1-(substituted phenyl)ethanol of formula I (wherein X represents a Cl or Br atom and R1, R2, and R3 may be the same or different and each represents H, a halogen atom, a C1-5 alkyl group, a C1-5 haloalkyl group, a C1-5 alkoxy group, a CN group, or a NO2 group, with the proviso that when 2 of R1, R2 and R3 are alkyl groups or alkoxy groups, they may be combined together to form a ring and that all of R1, R2, and R3 are not H atoms at the same time). ..
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