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
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
Approval Year
PubMed
Title | Date | PubMed |
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p-Cymene catabolic pathway in Pseudomonas putida F1: cloning and characterization of DNA encoding conversion of p-cymene to p-cumate. | 1997 May |
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Inhibitory effects on mushroom tyrosinase by some alkylbenzaldehydes. | 2003 Dec |
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Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae. | 2004 Jan |
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Percutaneous permeation enhancement by terpenes: mechanistic view. | 2008 |
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Toxicity of plant essential oils and their components against Lycoriella ingenua (Diptera: Sciaridae). | 2008 Feb |
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Activity of essential oils and individual components against acetyl- and butyrylcholinesterase. | 2008 Jul-Aug |
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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 |
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Classification Tree | Code System | Code | ||
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EPA PESTICIDE CODE |
115809
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JECFA EVALUATION |
CUMINALDEHYDE
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CFR |
21 CFR 172.515
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Code System | Code | Type | Description | ||
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2177095
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28671
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C007165
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204-516-9
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4886
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763
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122-03-2
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m3881
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DTXSID9021974
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O0893NC35F
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326
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CUMINALDEHYDE
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SUBSTANCE RECORD