CHEBI:31832 - methyl salicylate

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ChEBI Name methyl salicylate
ChEBI ID CHEBI:31832
Definition A benzoate ester that is the methyl ester of salicylic acid.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C8H8O3
Net Charge 0
Average Mass 152.14730
Monoisotopic Mass 152.047
InChI InChI=1S/C8H8O3/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5,9H,1H3
InChIKey OSWPMRLSEDHDFF-UHFFFAOYSA-N
SMILES COC(=O)c1ccccc1O
Roles Classification
Biological Role(s): flavouring agent
A food additive that is used to added improve the taste or odour of a food.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
insect attractant
A chemical that lures insects to a trap, thereby removing them from crops, animals or stored products.
Application(s): flavouring agent
A food additive that is used to added improve the taste or odour of a food.
insect attractant
A chemical that lures insects to a trap, thereby removing them from crops, animals or stored products.
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ChEBI Ontology
Outgoing methyl salicylate (CHEBI:31832) has functional parent salicylic acid (CHEBI:16914)
methyl salicylate (CHEBI:31832) has role flavouring agent (CHEBI:35617)
methyl salicylate (CHEBI:31832) has role insect attractant (CHEBI:24850)
methyl salicylate (CHEBI:31832) has role metabolite (CHEBI:25212)
methyl salicylate (CHEBI:31832) is a benzoate ester (CHEBI:36054)
methyl salicylate (CHEBI:31832) is a salicylates (CHEBI:26596)
Synonyms Sources
2-(Methoxycarbonyl)phenol ChemIDplus
2-Carbomethoxyphenol ChemIDplus
2-Hydroxybenzoic acid methyl ester ChemIDplus
Betula oil ChemIDplus
Gaultheria oil ChemIDplus
Methyl 2-hydroxybenzoate KEGG COMPOUND
Methyl o-hydroxybenzoate ChemIDplus
methyl salicylate UniProt
Natural wintergreen oil ChemIDplus
Oil of wintergreen ChemIDplus
Spicewood Oil ChemIDplus
Sweet birch oil ChemIDplus
Teaberry oil ChemIDplus
Database Links Databases
4245 DrugCentral
C00030767 KNApSAcK
C12305 KEGG COMPOUND
D01087 KEGG DRUG
Methyl_salicylate Wikipedia
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Registry Numbers Types Sources
119-36-8 CAS Registry Number NIST Chemistry WebBook
119-36-8 CAS Registry Number ChemIDplus
971516 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21249432 PubMed citation Europe PMC
21287406 PubMed citation Europe PMC
21327960 PubMed citation Europe PMC
21404848 PubMed citation Europe PMC
21609308 PubMed citation Europe PMC
21790190 PubMed citation Europe PMC
21936953 PubMed citation Europe PMC
Last Modified
22 February 2017