CHEBI:955 - 2,6-dimethoxyphenol

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ChEBI Name 2,6-dimethoxyphenol
Definition A member of the class of phenols that is phenol substituted by methoxy groups at positions 2 and 6.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C8H10O3
Net Charge 0
Average Mass 154.16320
Monoisotopic Mass 154.06299
InChI InChI=1S/C8H10O3/c1-10-6-4-3-5-7(11-2)8(6)9/h3-5,9H,1-2H3
SMILES COc1cccc(OC)c1O
Metabolite of Species Details
Panax japonicus var. major (NCBI:txid45211) Found in root (BTO:0001188). Ethanolic extract of dried and pulverized roots See: PubMed
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.
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ChEBI Ontology
Outgoing 2,6-dimethoxyphenol (CHEBI:955) has role plant metabolite (CHEBI:76924)
2,6-dimethoxyphenol (CHEBI:955) is a dimethoxybenzene (CHEBI:51681)
2,6-dimethoxyphenol (CHEBI:955) is a phenols (CHEBI:33853)
Incoming 2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-7H-pyrano[2,3-g][1,4]benzodioxin-7-one (CHEBI:91204) has functional parent 2,6-dimethoxyphenol (CHEBI:955)
Synonyms Sources
1,3-di-O-methylpyrogallol ChemIDplus
1,3-dimethoxy-2-hydroxybenzene ChemIDplus
1,3-dimethyl pyrogallate NIST Chemistry WebBook
2,6-Dimethoxyphenol KEGG COMPOUND
2-hydroxy-1,3-dimethoxybenzene ChemIDplus
Pyrogallol 1,3-dimethyl ether KEGG COMPOUND
Syringol ChemIDplus
Manual Xrefs Databases
3DM PDBeChem
C00002646 KNApSAcK
CPD-12797 MetaCyc
HMDB0034158 HMDB
Syringol Wikipedia
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Registry Numbers Types Sources
1526871 Reaxys Registry Number Reaxys
1526871 Beilstein Registry Number Beilstein
794071 Gmelin Registry Number Gmelin
91-10-1 CAS Registry Number NIST Chemistry WebBook
91-10-1 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11589408 PubMed citation Europe PMC
21417387 PubMed citation Europe PMC
25614246 PubMed citation Europe PMC
Last Modified
14 July 2016