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Details

Stereochemistry RACEMIC
Molecular Formula C8H9ClO
Molecular Weight 156.609
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-CHLORO-1-PHENYLETHANOL

SMILES

OC(CCl)C1=CC=CC=C1

InChI

InChIKey=XWCQSILTDPAWDP-UHFFFAOYSA-N
InChI=1S/C8H9ClO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6H2

HIDE SMILES / InChI

Molecular Formula C8H9ClO
Molecular Weight 156.609
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Bioreduction of alpha-chloroacetophenone by whole cells of marine fungi.
2009 Oct
Isolation of a Bacillus strain producing ketone reductase with high substrate tolerance.
2010 Feb
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 07:57:32 GMT 2023
Edited
by admin
on Sat Dec 16 07:57:32 GMT 2023
Record UNII
78M3294M16
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-CHLORO-1-PHENYLETHANOL
Systematic Name English
(CHLOROMETHYL)PHENYL CARBINOL
Systematic Name English
BENZYL ALCOHOL, .ALPHA.-(CHLOROMETHYL)-
Systematic Name English
.ALPHA.-(CHLOROMETHYL)BENZYL ALCOHOL
Systematic Name English
2-CHLORO-1-HYDROXY-1-PHENYLETHANE
Systematic Name English
STYRENE CHLOROHYDRIN
Common Name English
BENZENEMETHANOL, .ALPHA.-(CHLOROMETHYL)-
Systematic Name English
.ALPHA.-(CHLOROMETHYL)BENZENEMETHANOL
Systematic Name English
2-CHLORO-1-PHENYLETHANOL, (±)-
Systematic Name English
(±)-2-CHLORO-1-PHENYLETHANOL
Systematic Name English
1-PHENYL-2-CHLOROETHANOL
Systematic Name English
J28.520J
Code English
ALPHA-(CHLOROMETHYL)BENZYL ALCOHOL
Systematic Name English
STYRENE .BETA.-CHLOROHYDRIN
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID40937321
Created by admin on Sat Dec 16 07:57:32 GMT 2023 , Edited by admin on Sat Dec 16 07:57:32 GMT 2023
PRIMARY
PUBCHEM
92898
Created by admin on Sat Dec 16 07:57:32 GMT 2023 , Edited by admin on Sat Dec 16 07:57:32 GMT 2023
PRIMARY
FDA UNII
78M3294M16
Created by admin on Sat Dec 16 07:57:32 GMT 2023 , Edited by admin on Sat Dec 16 07:57:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
216-816-7
Created by admin on Sat Dec 16 07:57:32 GMT 2023 , Edited by admin on Sat Dec 16 07:57:32 GMT 2023
PRIMARY
CAS
1674-30-2
Created by admin on Sat Dec 16 07:57:32 GMT 2023 , Edited by admin on Sat Dec 16 07:57:32 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE