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Details

Stereochemistry RACEMIC
Molecular Formula C9H10O
Molecular Weight 134.1751
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-BENZYLOXIRANE

SMILES

C(C1CO1)C2=CC=CC=C2

InChI

InChIKey=JFDMLXYWGLECEY-UHFFFAOYSA-N
InChI=1S/C9H10O/c1-2-4-8(5-3-1)6-9-7-10-9/h1-5,9H,6-7H2

HIDE SMILES / InChI

Molecular Formula C9H10O
Molecular Weight 134.1751
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Laboratory-Evolved Enzymes Provide Snapshots of the Development of Enantioconvergence in Enzyme-Catalyzed Epoxide Hydrolysis.
2016-09-15
Substance Class Chemical
Created
by admin
on Wed Apr 02 11:18:46 GMT 2025
Edited
by admin
on Wed Apr 02 11:18:46 GMT 2025
Record UNII
LKQ2758W1E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-4327
Preferred Name English
2-BENZYLOXIRANE
Common Name English
OXIRANE, 2-(PHENYLMETHYL)-
Systematic Name English
(2,3-EPOXYPROPYL)BENZENE, (±)-
Systematic Name English
3-PHENYLPROPENE-1,2-OXIDE
Systematic Name English
(2,3-EPOXYPROPYL)BENZENE
Systematic Name English
1-PHENYL-2,3-EPOXYPROPANE
Systematic Name English
ALLYLBENZENE 2',3'-OXIDE
Systematic Name English
BENZENE, (2,3-EPOXYPROPYL)-
Systematic Name English
2-(PHENYLMETHYL)OXIRANE
Systematic Name English
2,3-EPOXY-1-PHENYLPROPANE
Systematic Name English
Code System Code Type Description
CAS
4436-24-2
Created by admin on Wed Apr 02 11:18:46 GMT 2025 , Edited by admin on Wed Apr 02 11:18:46 GMT 2025
PRIMARY
FDA UNII
LKQ2758W1E
Created by admin on Wed Apr 02 11:18:46 GMT 2025 , Edited by admin on Wed Apr 02 11:18:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID501032201
Created by admin on Wed Apr 02 11:18:46 GMT 2025 , Edited by admin on Wed Apr 02 11:18:46 GMT 2025
PRIMARY
PUBCHEM
94826
Created by admin on Wed Apr 02 11:18:46 GMT 2025 , Edited by admin on Wed Apr 02 11:18:46 GMT 2025
PRIMARY
NSC
4327
Created by admin on Wed Apr 02 11:18:46 GMT 2025 , Edited by admin on Wed Apr 02 11:18:46 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE