CHEBI:138129 - rac-6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name rac-6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid
ChEBI ID CHEBI:138129
ChEBI ASCII Name rac-6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid
Definition A racemate comprising equimolar amounts of the R- and S- enantiomers of 6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid. It is the minor component of the herbicide imazamethabenz.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C15H18N2O3
Net Charge 0
Average Mass 274.316
Monoisotopic Mass 274.13174
InChI InChI=1S/C15H18N2O3/c1-8(2)15(4)14(20)16-12(17-15)11-7-9(3)5-6-10(11)13(18)19/h5-8H,1-4H3,(H,18,19)(H,16,17,20)
InChIKey KFEFNHNXZQYTEW-UHFFFAOYSA-N
SMILES C(O)(C1=C(C=C(C=C1)C)C2=NC(C(N2)=O)(C(C)C)C)=O
ChEBI Ontology
Outgoing rac-6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid (CHEBI:138129) has part 6-[(4R)-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]-p-toluic acid (CHEBI:138127)
rac-6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid (CHEBI:138129) has part 6-[(4S)-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]-p-toluic acid (CHEBI:138128)
rac-6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid (CHEBI:138129) is a racemate (CHEBI:60911)
Incoming imazamethabenz (CHEBI:138116) has part rac-6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluic acid (CHEBI:138129)
IUPAC Name
rac-2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-4-methylbenzoic acid
Synonyms Sources
6-[(RS)-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]-p-toluic acid ChEBI
p-imazamethabenz ChEBI
p-imazamethabenz acid ChEBI
p-imazamethabenz-acid ChEBI
para-imazamethabenz ChEBI
para-imazamethabenz acid ChEBI
para-imazamethabenz-acid ChEBI
rac-2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl)-4-methylbenzoic acid ChemIDplus
Registry Numbers Types Sources
8329358 Reaxys Registry Number Reaxys
89318-82-1 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
9435470 PubMed citation Europe PMC
Last Modified
10 August 2017