U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C10H12O
Molecular Weight 148.2017
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CUMINALDEHYDE

SMILES

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

InChI

InChIKey=WTWBUQJHJGUZCY-UHFFFAOYSA-N
InChI=1S/C10H12O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-8H,1-2H3

HIDE SMILES / InChI

Molecular Formula C10H12O
Molecular Weight 148.2017
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
p-Cymene catabolic pathway in Pseudomonas putida F1: cloning and characterization of DNA encoding conversion of p-cymene to p-cumate.
1997 May
Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae.
2004 Jan
Acaricidal and quantitative structure activity relationship of monoterpenes against the two-spotted spider mite, Tetranychus urticae.
2010 Nov
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:17:55 GMT 2023
Edited
by admin
on Fri Dec 15 16:17:55 GMT 2023
Record UNII
O0893NC35F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CUMINALDEHYDE
FHFI   MI  
Systematic Name English
CUMINIC ALDEHYDE
FCC  
Common Name English
CUMALDEHYDE
Systematic Name English
NSC-4886
Code English
CUMINIC ALDEHYDE [FCC]
Common Name English
CUMINALDEHYDE [MI]
Common Name English
P-CUMINIC ALDEHYDE
Common Name English
BENZALDEHYDE, 4-(1-METHYLETHYL)-
Systematic Name English
4-ISOPROPYLBENZALDEHYDE
Systematic Name English
4-I-PROPYLBENZALDEHYDE
Common Name English
FEMA NO. 2341
Code English
P-CUMIC ALDEHYDE
Common Name English
4-(1-METHYLETHYL)BENZALDEHYDE
Systematic Name English
CUMINAL
Systematic Name English
CUMINALDEHYDE [FHFI]
Common Name English
P-ISOPROPYLBENZALDEHYDE
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 115809
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
JECFA EVALUATION CUMINALDEHYDE
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
Code System Code Type Description
RXCUI
2177095
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
CHEBI
28671
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
MESH
C007165
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-516-9
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
NSC
4886
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
JECFA MONOGRAPH
763
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
CAS
122-03-2
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
MERCK INDEX
m3881
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID9021974
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
FDA UNII
O0893NC35F
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
PUBCHEM
326
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
WIKIPEDIA
CUMINALDEHYDE
Created by admin on Fri Dec 15 16:17:55 GMT 2023 , Edited by admin on Fri Dec 15 16:17:55 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
Pure compound identified in the Paeonia lactiflora (Paeoniaceae) root steam distillate with growth-inhibiting activity against nine harmful intestinal bacteria and eight lactic acid-producing bacteria.