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more general categories	information about this item
04. Bioactive Capabilities of Specific Chemicals	04. Bioactive Capabilities of Specific Chemicals
Oxidoreductases [EC:1] (1697)
Acting on the CH-OH group of donors [EC:1.1] (576)
With NAD or NADP as acceptor [EC:1.1.1] (507)
Sulcatone reductase [EC:1.1.1.260] (5)	sulcatol [CHEBI:15833] (1)
08. Chemical Category	08. Chemical Category
main group molecular entity [CHEBI:33579] (25650)
s-block molecular entity [CHEBI:33674] (7287)
hydrogen molecular entity [CHEBI:33608] (6932)
hydroxides [CHEBI:24651] (5641)
organic hydroxy compound [CHEBI:33822] (3050)
alcohol [CHEBI:30879] (1371)
secondary alcohol [CHEBI:35681] (342)	sulcatol [CHEBI:15833] (1)
p-block molecular entity [CHEBI:33675] (25343)
chalcogen molecular entity [CHEBI:33304] (15225)
oxygen molecular entity [CHEBI:25806] (14414)
hydroxides [CHEBI:24651] (5641)
organic hydroxy compound [CHEBI:33822] (3050)
alcohol [CHEBI:30879] (1371)
secondary alcohol [CHEBI:35681] (342)	sulcatol [CHEBI:15833] (1)
carbon group molecular entity [CHEBI:33582] (23847)
organic molecular entity [CHEBI:50860] (23769)
organic hydroxy compound [CHEBI:33822] (3050)
alcohol [CHEBI:30879] (1371)
secondary alcohol [CHEBI:35681] (342)	sulcatol [CHEBI:15833] (1)
polyatomic entity [CHEBI:36357] (18777)
heteroatomic molecular entity [CHEBI:37577] (13672)
hydroxides [CHEBI:24651] (5641)
organic hydroxy compound [CHEBI:33822] (3050)
alcohol [CHEBI:30879] (1371)
secondary alcohol [CHEBI:35681] (342)	sulcatol [CHEBI:15833] (1)
ChEBI Compound Accession Identifier:	[CHEBI:15833]
ChEBI Compound Description:	null
ChEBI Compound Identification Number:	15833
ChEBI InChI Value:	InChI=1S/C8H16O/c1-7(2)5-4-6-8(3)9/h5,8-9H,4,6H2,1-3H3
ChEBI InChIKey Value:	OHEFFKYYKJVVOX-UHFFFAOYSA-N
ChEBI Compound Name:	sulcatol
ChEBI SMILES Value:	CC(O)CCC=C(C)C
ChEBI Substance ID:	8145112
ChEBI URL:	ChEBI:15833
ChemSpider ID:	19533
Ontomatica Chemical Accession Key (OnChAKey):	OHEFFKYYKJVVOX_UHFFFAOYSA_N_000_000000
PubChem Compound ID:	20745