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Details

Stereochemistry RACEMIC
Molecular Formula C15H18N2O3
Molecular Weight 274.315
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-(4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL)-5-METHYLBENZOIC ACID

SMILES

CC(C)C1(C)N=C(NC1=O)C2=CC=C(C)C=C2C(O)=O

InChI

InChIKey=LUZQQSLTOCTPIN-UHFFFAOYSA-N
InChI=1S/C15H18N2O3/c1-8(2)15(4)14(20)16-12(17-15)10-6-5-9(3)7-11(10)13(18)19/h5-8H,1-4H3,(H,18,19)(H,16,17,20)

HIDE SMILES / InChI

Molecular Formula C15H18N2O3
Molecular Weight 274.315
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Pesticides in surface drinking-water supplies of the northern Great Plains.
2007-08
Imidazolinone-tolerant crops: history, current status and future.
2005-03
Cross resistance to ALS-inhibiting herbicides in Euphorbia heterophylla L. biotypes resistant to imazethapyr.
2003
Evaluation of resistance in Amaranthus quitensis Kunth populations to imazethapyr and other imidazolinones.
2003
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:21:18 GMT 2025
Edited
by admin
on Mon Mar 31 22:21:18 GMT 2025
Record UNII
Z0LRW2M500
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-(4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL)-5-METHYLBENZOIC ACID
Systematic Name English
2-(4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL)-5-METHYLBENZOIC ACID (ISO)
Preferred Name English
BENZOIC ACID, 2-(4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL)-5-METHYL-
Systematic Name English
Code System Code Type Description
PUBCHEM
13884415
Created by admin on Mon Mar 31 22:21:18 GMT 2025 , Edited by admin on Mon Mar 31 22:21:18 GMT 2025
PRIMARY
CAS
89318-81-0
Created by admin on Mon Mar 31 22:21:18 GMT 2025 , Edited by admin on Mon Mar 31 22:21:18 GMT 2025
PRIMARY
EPA CompTox
DTXSID00274067
Created by admin on Mon Mar 31 22:21:18 GMT 2025 , Edited by admin on Mon Mar 31 22:21:18 GMT 2025
PRIMARY
FDA UNII
Z0LRW2M500
Created by admin on Mon Mar 31 22:21:18 GMT 2025 , Edited by admin on Mon Mar 31 22:21:18 GMT 2025
PRIMARY
CAS
100594-44-3
Created by admin on Mon Mar 31 22:21:18 GMT 2025 , Edited by admin on Mon Mar 31 22:21:18 GMT 2025
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