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Details

Stereochemistry ACHIRAL
Molecular Formula C6H4O4
Molecular Weight 140.0936
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of COUMALIC ACID

SMILES

OC(=O)C1=COC(=O)C=C1

InChI

InChIKey=ORGPJDKNYMVLFL-UHFFFAOYSA-N
InChI=1S/C6H4O4/c7-5-2-1-4(3-10-5)6(8)9/h1-3H,(H,8,9)

HIDE SMILES / InChI

Molecular Formula C6H4O4
Molecular Weight 140.0936
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Stimulation by caffeic acid, coumalic acid, and corilagin of the germination of resting spores of the clubroot pathogen Plasmodiophora brassicae.
2003-01
Characterization and expression of enzymatically active recombinant filarial prolyl 4-hydroxylase.
2001-09-03
Inhibition of HIV-1 proteinase by non-peptide carboxylates.
1991-04-15
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:22:12 GMT 2025
Edited
by admin
on Mon Mar 31 21:22:12 GMT 2025
Record UNII
OB1JPY343G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-22978
Preferred Name English
COUMALIC ACID
MI  
Common Name English
2-PENTENEDIOIC ACID, 4-(HYDROXYMETHYLENE)-, .DELTA.-LACTONE
Common Name English
2-OXO-1(2H)-PYRAN-5-CARBOXYLIC ACID
Common Name English
GLUTACONIC ACID, 4-(HYDROXYMETHYLENE)-, .DELTA.-LACTONE
Common Name English
.ALPHA.-PYRONE-5-CARBOXYLIC ACID
Common Name English
CUMALIC ACID
Common Name English
2-OXOPYRAN-5-CARBOXYLIC ACID
Systematic Name English
COUMALIC ACID [MI]
Common Name English
2-OXO-2H-PYRAN-5-CARBOXYLIC ACID
Systematic Name English
Code System Code Type Description
CAS
500-05-0
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
PRIMARY
MERCK INDEX
m3815
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
PRIMARY Merck Index
NSC
22978
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-899-0
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID60870569
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
PRIMARY
PUBCHEM
68141
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
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WIKIPEDIA
Coumalic acid
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
PRIMARY
FDA UNII
OB1JPY343G
Created by admin on Mon Mar 31 21:22:12 GMT 2025 , Edited by admin on Mon Mar 31 21:22:12 GMT 2025
PRIMARY