U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C15H13NO2
Molecular Weight 239.2692
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-BIS(P-HYDROXYPHENYL)PROPIONITRILE

SMILES

OC1=CC=C(CC(C#N)C2=CC=C(O)C=C2)C=C1

InChI

InChIKey=GHZHWDWADLAOIQ-UHFFFAOYSA-N
InChI=1S/C15H13NO2/c16-10-13(12-3-7-15(18)8-4-12)9-11-1-5-14(17)6-2-11/h1-8,13,17-18H,9H2

HIDE SMILES / InChI

Molecular Formula C15H13NO2
Molecular Weight 239.2692
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:31:17 UTC 2023
Edited
by admin
on Sat Dec 16 17:31:17 UTC 2023
Record UNII
52XWB8Q4V8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3-BIS(P-HYDROXYPHENYL)PROPIONITRILE
Systematic Name English
DPN
Common Name English
4-HYDROXY-.ALPHA.-(4-HYDROXYPHENYL)BENZENEPROPANENITRILE
Systematic Name English
BENZENEPROPANENITRILE, 4-HYDROXY-.ALPHA.-(4-HYDROXYPHENYL)-
Systematic Name English
DIARYLPROPIONITRILE
Common Name English
2,3-BIS(4-HYDROXYPHENYL)PROPANENITRILE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
Diarylpropionitrile
Created by admin on Sat Dec 16 17:31:18 UTC 2023 , Edited by admin on Sat Dec 16 17:31:18 UTC 2023
PRIMARY
CHEBI
63949
Created by admin on Sat Dec 16 17:31:18 UTC 2023 , Edited by admin on Sat Dec 16 17:31:18 UTC 2023
PRIMARY
CAS
1428-67-7
Created by admin on Sat Dec 16 17:31:18 UTC 2023 , Edited by admin on Sat Dec 16 17:31:18 UTC 2023
PRIMARY
EPA CompTox
DTXSID0040387
Created by admin on Sat Dec 16 17:31:18 UTC 2023 , Edited by admin on Sat Dec 16 17:31:18 UTC 2023
PRIMARY
FDA UNII
52XWB8Q4V8
Created by admin on Sat Dec 16 17:31:18 UTC 2023 , Edited by admin on Sat Dec 16 17:31:18 UTC 2023
PRIMARY
PUBCHEM
102614
Created by admin on Sat Dec 16 17:31:18 UTC 2023 , Edited by admin on Sat Dec 16 17:31:18 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE