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Details

Stereochemistry ACHIRAL
Molecular Formula C10H7NO4
Molecular Weight 205.1669
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-(CARBOXYMETHYL)PHTHALIMIDE

SMILES

OC(=O)CN1C(=O)C2=C(C=CC=C2)C1=O

InChI

InChIKey=WQINSVOOIJDOLJ-UHFFFAOYSA-N
InChI=1S/C10H7NO4/c12-8(13)5-11-9(14)6-3-1-2-4-7(6)10(11)15/h1-4H,5H2,(H,12,13)

HIDE SMILES / InChI

Molecular Formula C10H7NO4
Molecular Weight 205.1669
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
(2R)-2-(1,3-Dioxoisoindolin-2-yl)-4-(methyl-sulfan-yl)butanoic acid.
2009-07-25
Synthesis and anticonvulsant activity of N,N-phthaloyl derivatives of central nervous system inhibitory amino acids.
2001-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:48:56 GMT 2025
Edited
by admin
on Mon Mar 31 18:48:56 GMT 2025
Record UNII
6J5LY4N0CG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-(CARBOXYMETHYL)PHTHALIMIDE
Systematic Name English
NSC-10771
Preferred Name English
2-PHTHALIMIDOACETIC ACID
Systematic Name English
N-PHTHALYLGLYCINE
Common Name English
2-ISOINDOLINEACETIC ACID, 1,3-DIOXO-
Common Name English
2H-ISOINDOLE-2-ACETIC ACID, 1,3-DIHYDRO-1,3-DIOXO-
Systematic Name English
PHTHALIMIDOACETIC ACID
Systematic Name English
NSC-29044
Code English
PHTHALYLGLYCINE, N-
Common Name English
Code System Code Type Description
NSC
10771
Created by admin on Mon Mar 31 18:48:56 GMT 2025 , Edited by admin on Mon Mar 31 18:48:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID00197005
Created by admin on Mon Mar 31 18:48:56 GMT 2025 , Edited by admin on Mon Mar 31 18:48:56 GMT 2025
PRIMARY
PUBCHEM
20825
Created by admin on Mon Mar 31 18:48:56 GMT 2025 , Edited by admin on Mon Mar 31 18:48:56 GMT 2025
PRIMARY
NSC
29044
Created by admin on Mon Mar 31 18:48:56 GMT 2025 , Edited by admin on Mon Mar 31 18:48:56 GMT 2025
PRIMARY
ECHA (EC/EINECS)
225-177-3
Created by admin on Mon Mar 31 18:48:56 GMT 2025 , Edited by admin on Mon Mar 31 18:48:56 GMT 2025
PRIMARY
FDA UNII
6J5LY4N0CG
Created by admin on Mon Mar 31 18:48:56 GMT 2025 , Edited by admin on Mon Mar 31 18:48:56 GMT 2025
PRIMARY
CAS
4702-13-0
Created by admin on Mon Mar 31 18:48:56 GMT 2025 , Edited by admin on Mon Mar 31 18:48:56 GMT 2025
PRIMARY