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CHEBI:142604 - (E)-non-2-en-1-ol

ChEBI IDCHEBI:142604
ChEBI Name(E)-non-2-en-1-ol
Stars
ASCII Name(E)-non-2-en-1-ol
DefinitionA medium-chain primary fatty alcohol that is (E)-non-2-ene carrying a hydroxy group at position 1.
Last Modified1 July 2019
SubmitterAnne Morgat
DownloadsMolfile
FormulaC9H18O
Net Charge0
Average Mass142.242
Monoisotopic Mass142.13577
SMILESCCCCCC/C=C/CO
InChIInChI=1S/C9H18O/c1-2-3-4-5-6-7-8-9-10/h7-8,10H,2-6,9H2,1H3/b8-7+
InChIKeyNSSALFVIQPAIQK-BQYQJAHWSA-N
Species of MetaboliteComponentSourceComments
Hippophae rhamnoides subsp. sinensis (ncbitaxon:193531) stem (BTO:0001300) PubMed (22888528)
Hordeum vulgare (ncbitaxon:4513) root (BTO:0001188) PubMed (23793896)
Solea senegalensis (ncbitaxon:28829) - DOI ( 10.1016/j.foodchem.2011.09.035)
Roles Classification
Biological Roles:
pheromone  A semiochemical used in olfactory communication between organisms of the same species eliciting a change in sexual or social behaviour.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
flavouring agent  A food additive that is used to added improve the taste or odour of a food.
Application:
flavouring agent  A food additive that is used to added improve the taste or odour of a food.
ChEBI Ontology
Outgoing Relation(s)
(E)-non-2-en-1-ol (CHEBI:142604) has role flavouring agent (CHEBI:35617)
(E)-non-2-en-1-ol (CHEBI:142604) has role pheromone (CHEBI:26013)
(E)-non-2-en-1-ol (CHEBI:142604) has role plant metabolite (CHEBI:76924)
(E)-non-2-en-1-ol (CHEBI:142604) is a medium-chain primary fatty alcohol (CHEBI:142605)
(E)-non-2-en-1-ol (CHEBI:142604) is a primary allylic alcohol (CHEBI:134394)
(E)-non-2-en-1-ol (CHEBI:142604) is a volatile organic compound (CHEBI:134179)
Incoming Relation(s)
(E)-non-2-enoic acid (CHEBI:143910) has functional parent (E)-non-2-en-1-ol (CHEBI:142604)
IUPAC Name 
(2E)-non-2-en-1-ol
Synonyms  Source
(E)-non-2-enolSUBMITTER
(E)-2-nonen-1-olFooDB
(E)-2-nonenolSUBMITTER
(2E)-2-nonen-1-olChemIDplus
trans-2-nonen-1-olChemIDplus
trans-2-nonenolFooDB
UniProt Name  Source
(E)-non-2-en-1-olUniProt
Manual XrefsDatabases
HMDB0041498HMDB
LMFA05000131LIPID MAPS
FDB021469FooDB
Registry NumbersSources
Reaxys:1701076Reaxys
CAS:31502-14-4ChemIDplus
CAS:31502-14-4NIST Chemistry WebBook
Citations