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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:33227 - (
E
)-cinnamyl alcohol
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ChEBI Name
(
E
)-cinnamyl alcohol
ChEBI ID
CHEBI:33227
ChEBI ASCII Name
(E)-cinnamyl alcohol
Definition
The
E
(
trans
) stereoisomer of cinnamyl alcohol.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C9H10O
Net Charge
0
Average Mass
134.17510
Monoisotopic Mass
134.07316
InChI
InChI=1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-7,10H,8H2/b7-4+
InChIKey
OOCCDEMITAIZTP-QPJJXVBHSA-N
SMILES
OC\C=C\c1ccccc1
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.
(via
cinnamyl alcohol
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
has role
plant metabolite (
CHEBI:76924
)
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
is a
cinnamyl alcohol (
CHEBI:17177
)
Incoming
(
E
)-5-hydroxyconiferyl alcohol (
CHEBI:31135
)
has functional parent
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
(
E
)-caffeyl alcohol (
CHEBI:31334
)
has functional parent
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
3,4,5-trimethoxy cinnamyl alcohol (
CHEBI:86546
)
has functional parent
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
3,4-dimethoxycinnamyl alcohol (
CHEBI:86551
)
has functional parent
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
trans
-
p
-coumaryl alcohol (
CHEBI:64555
)
has functional parent
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
coniferol (
CHEBI:17745
)
has functional parent
(
E
)-cinnamyl alcohol (
CHEBI:33227
)
IUPAC Name
(2
E
)-3-phenylprop-2-en-1-ol
Synonyms
Sources
(
E
)-3-phenyl-2-propen-1-ol
ChemIDplus
(
E
)-cinnamyl alcohol
UniProt
3-Phenyl-2-propen-1-ol
KEGG COMPOUND
Styrylcarbinol
KEGG COMPOUND
Manual Xrefs
Databases
C02394
KEGG COMPOUND
CINNAMYL-ALC
MetaCyc
Cinnamyl_alcohol
Wikipedia
HMDB0029698
HMDB
View more database links
Registry Numbers
Types
Sources
104-54-1
CAS Registry Number
KEGG COMPOUND
261108
Gmelin Registry Number
Gmelin
4407-36-7
CAS Registry Number
NIST Chemistry WebBook
4407-36-7
CAS Registry Number
ChemIDplus
741973
Reaxys Registry Number
Reaxys
Citations
Types
Sources
20431333
PubMed citation
Europe PMC
20940038
PubMed citation
Europe PMC
Last Modified
20 July 2015