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Details

Stereochemistry RACEMIC
Molecular Formula C8H9NO2
Molecular Weight 151.1626
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MANDELAMIDE, (±)-

SMILES

NC(=O)C(O)C1=CC=CC=C1

InChI

InChIKey=MAGPZHKLEZXLNU-UHFFFAOYSA-N
InChI=1S/C8H9NO2/c9-8(11)7(10)6-4-2-1-3-5-6/h1-5,7,10H,(H2,9,11)

HIDE SMILES / InChI

Molecular Formula C8H9NO2
Molecular Weight 151.1626
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 12:39:49 GMT 2023
Edited
by admin
on Sat Dec 16 12:39:49 GMT 2023
Record UNII
I5M132OPVN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MANDELAMIDE, (±)-
Common Name English
MANDELAMIDE
Common Name English
2-HYDROXY-2-PHENYLACETAMIDE
Systematic Name English
AMYGDALINAMIDE
Common Name English
.ALPHA.-HYDROXYBENZYLCARBOXAMIDE
Common Name English
2-PHENYLGLYCOLAMIDE
Systematic Name English
(±)-MANDELAMIDE
Common Name English
DL-MANDELIC ACID AMIDE
Common Name English
NSC-16603
Code English
BENZENEACETAMIDE, .ALPHA.-HYDROXY-
Systematic Name English
Code System Code Type Description
FDA UNII
I5M132OPVN
Created by admin on Sat Dec 16 12:39:49 GMT 2023 , Edited by admin on Sat Dec 16 12:39:49 GMT 2023
PRIMARY
CHEBI
136824
Created by admin on Sat Dec 16 12:39:49 GMT 2023 , Edited by admin on Sat Dec 16 12:39:49 GMT 2023
PRIMARY
CAS
4410-31-5
Created by admin on Sat Dec 16 12:39:49 GMT 2023 , Edited by admin on Sat Dec 16 12:39:49 GMT 2023
PRIMARY
PUBCHEM
73558
Created by admin on Sat Dec 16 12:39:49 GMT 2023 , Edited by admin on Sat Dec 16 12:39:49 GMT 2023
PRIMARY
NSC
16603
Created by admin on Sat Dec 16 12:39:49 GMT 2023 , Edited by admin on Sat Dec 16 12:39:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID901318287
Created by admin on Sat Dec 16 12:39:49 GMT 2023 , Edited by admin on Sat Dec 16 12:39:49 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE