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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
Competitive inhibition of mushroom tyrosinase by 4-substituted benzaldehydes.
2001 Aug
Inhibitory effects on mushroom tyrosinase by some alkylbenzaldehydes.
2003 Dec
QSAR and kinetics of the inhibition of benzaldehyde derivatives against Sacrophaga neobelliaria phenoloxidase.
2004 Feb 15
Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae.
2004 Jan
Cuminaldehyde: Aldose Reductase and alpha-Glucosidase Inhibitor Derived from Cuminum cyminum L. Seeds.
2005 Apr 6
Biotransformation of terpenoids by mammals, microorganisms, and plant-cultured cells.
2005 May
Antifungal effects of volatile compounds from black zira (Bunium persicum) and other spices and herbs.
2007 Nov
Percutaneous permeation enhancement by terpenes: mechanistic view.
2008
Toxicity of plant essential oils and their components against Lycoriella ingenua (Diptera: Sciaridae).
2008 Feb
2-(4-Isopropyl-benzylidene)propanoic acid.
2008 Jul 12
Activity of essential oils and individual components against acetyl- and butyrylcholinesterase.
2008 Jul-Aug
Effects of cuminaldehyde on melanoma cells.
2008 Jun
Fumigant and contact toxicities of monoterpenes to Sitophilus oryzae (L.) and Tribolium castaneum (Herbst) and their inhibitory effects on acetylcholinesterase activity.
2009 May
Cytochrome P450-catalysed arene-epoxidation of the bioactive tea tree oil ingredient p-cymene: indication for the formation of a reactive allergenic intermediate?
2009 Sep
Bioactivity of major components from the seeds of Bunium persicum (Boiss.) Fedtch.
2010 Jul
Enhanced repellency of binary mixtures of Zanthoxylum piperitum pericarp steam distillate or Zanthoxylum armatum seed oil constituents and Calophyllum inophyllum nut oil and their aerosols to Stomoxys calcitrans.
2010 Nov
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 UTC 2023
Edited
by admin
on Fri Dec 15 16:17:55 UTC 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 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
JECFA EVALUATION CUMINALDEHYDE
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
Code System Code Type Description
RXCUI
2177095
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
CHEBI
28671
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
MESH
C007165
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-516-9
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
NSC
4886
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
JECFA MONOGRAPH
763
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
CAS
122-03-2
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
MERCK INDEX
m3881
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID9021974
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
FDA UNII
O0893NC35F
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
PUBCHEM
326
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
WIKIPEDIA
CUMINALDEHYDE
Created by admin on Fri Dec 15 16:17:55 UTC 2023 , Edited by admin on Fri Dec 15 16:17:55 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
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