CHEBI:42438 - 2-methoxy-4-vinylphenol

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ChEBI Name 2-methoxy-4-vinylphenol
ChEBI ID CHEBI:42438
Definition A member of the class of phenols that is guaiacol in which the hydrogen para- to the hydroxy group is replaced by a vinyl group.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C9H10O2
Net Charge 0
Average Mass 150.17450
Monoisotopic Mass 150.06808
InChI InChI=1S/C9H10O2/c1-3-7-4-5-8(10)9(6-7)11-2/h3-6,10H,1H2,2H3
InChIKey YOMSJEATGXXYPX-UHFFFAOYSA-N
SMILES COc1cc(C=C)ccc1O
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
pheromone
A semiochemical used in olfactory communication between organisms of the same species eliciting a change in sexual or social behaviour.
flavouring agent
A food additive that is used to added improve the taste or odour of a food.
Application(s): flavouring agent
A food additive that is used to added improve the taste or odour of a food.
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ChEBI Ontology
Outgoing 2-methoxy-4-vinylphenol (CHEBI:42438) has role flavouring agent (CHEBI:35617)
2-methoxy-4-vinylphenol (CHEBI:42438) has role pheromone (CHEBI:26013)
2-methoxy-4-vinylphenol (CHEBI:42438) has role plant metabolite (CHEBI:76924)
2-methoxy-4-vinylphenol (CHEBI:42438) is a phenols (CHEBI:33853)
IUPAC Name
4-ethenyl-2-methoxyphenol
Synonyms Sources
2-(4-hydroxy-3-methoxyphenyl)ethene ChEBI
2-methoxy-4-vinylphenol UniProt
2M4VP ChEBI
4-ethenyl-2-methoxyphenol NIST Chemistry WebBook
4-hydroxy-3-methoxyphenylethene ChEBI
4-hydroxy-3-methoxystyrene ChemIDplus
4-hydroxy-3-methoxyvinylbenzene ChemIDplus
4-vinyl-2-methoxyphenol NIST Chemistry WebBook
4-vinylguaiacol ChemIDplus
o-methoxy-p-vinylphenol NIST Chemistry WebBook
p-vinylguaiacol NIST Chemistry WebBook
para-vinylguaiacol NIST Chemistry WebBook
Manual Xrefs Databases
2-Methoxy-4-vinylphenol Wikipedia
C17883 KEGG COMPOUND
CPD-1072 MetaCyc
DB03514 DrugBank
HMDB0013744 HMDB
HMDB0013819 HMDB
View more database links
Registry Numbers Types Sources
2044521 Reaxys Registry Number Reaxys
7786-61-0 CAS Registry Number NIST Chemistry WebBook
7786-61-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
18069243 PubMed citation Europe PMC
20816752 PubMed citation Europe PMC
22210037 PubMed citation Europe PMC
23461409 PubMed citation Europe PMC
24958143 PubMed citation Europe PMC
25574973 PubMed citation Europe PMC
Last Modified
02 September 2015