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Details

Stereochemistry ACHIRAL
Molecular Formula C10H12O2
Molecular Weight 164.2011
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CUMIC ACID

SMILES

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

InChI

InChIKey=CKMXAIVXVKGGFM-UHFFFAOYSA-N
InChI=1S/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12)

HIDE SMILES / InChI

Molecular Formula C10H12O2
Molecular Weight 164.2011
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Production of functionalized polyhydroxyalkanoates by genetically modified Methylobacterium extorquens strains.
2010-09-16
High-level recombinant protein production in CHO cells using lentiviral vectors and the cumate gene-switch.
2010-06-01
The study of some polyphenolic compounds from Melissa officinalis L. (Lamiaceae).
2009-03-20
A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases.
2008-04-03
High-level recombinant protein production in CHO cells using an adenoviral vector and the cumate gene-switch.
2007-02-03
Functional identification of p-cumate operons in the terpene-degrading Rhodococcus sp. strain T104.
2007-01
A study of chemical composition and antimicrobial activity of Bulgarian propolis.
2007
Identification and expression of the cym, cmt, and tod catabolic genes from Pseudomonas putida KL47: expression of the regulatory todST genes as a factor for catabolic adaptation.
2006-04
Expansion of growth substrate range in Pseudomonas putida F1 by mutations in both cymR and todS, which recruit a ring-fission hydrolase CmtE and induce the tod catabolic operon, respectively.
2003-03
Antifungal constituents of the stem bark of Bridelia retusa.
2003-02
Microsomal metabolism and enzyme kinetics of the terpene p-cymene in the common brushtail possum (Trichosurus vulpecula), koala (Phascolarctos cinereus) and rat.
2002-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:34 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:34 GMT 2025
Record UNII
6LP0WTM1JB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-1907
Preferred Name English
CUMIC ACID
MI  
Common Name English
4-(1-METHYLETHYL)BENZOIC ACID
Systematic Name English
P-ISOPROPYLBENZOIC ACID
Common Name English
CUMIC ACID [MI]
Common Name English
CUMINIC ACID
Common Name English
Code System Code Type Description
CAS
536-66-3
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
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FDA UNII
6LP0WTM1JB
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
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EPA CompTox
DTXSID6060210
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
PRIMARY
CHEBI
28122
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
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NSC
1907
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
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MERCK INDEX
m3878
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
PRIMARY Merck Index
PUBCHEM
10820
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
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MESH
C055607
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
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ECHA (EC/EINECS)
208-642-5
Created by admin on Mon Mar 31 19:56:34 GMT 2025 , Edited by admin on Mon Mar 31 19:56:34 GMT 2025
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