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Details

Stereochemistry RACEMIC
Molecular Formula C8H16O
Molecular Weight 128.212
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULCATOL

SMILES

CC(O)CCC=C(C)C

InChI

InChIKey=OHEFFKYYKJVVOX-UHFFFAOYSA-N
InChI=1S/C8H16O/c1-7(2)5-4-6-8(3)9/h5,8-9H,4,6H2,1-3H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Short anaerobiosis period prior to cold storage alleviates bitter pit and superficial scald in Granny Smith apples.
2010-09
Fragrance material review on 2-methyl-2-hepten-6-ol.
2010-01
Metabolomic change precedes apple superficial scald symptoms.
2009-09-23
Differentiation of the volatile profile of microbiologically contaminated canned tomatoes by dynamic headspace extraction followed by gas chromatography-mass spectrometry analysis.
2009-01-15
Lycopene accumulation affects the biosynthesis of some carotenoid-related volatiles independent of ethylene in tomato.
2008-08
Volatile composition in raspberry cultivars grown in the Pacific Northwest determined by stir bar sorptive extraction-gas chromatography-mass spectrometry.
2008-06-11
Significance of chirality in pheromone science.
2007-12-15
Can an inactivating agent increase enzyme activity in organic solvent? Effects of 18-crown-6 on lipase activity, enantioselectivity, and conformation.
2007-05-01
Mono- and disaccharides enhance the activity and enantioselectivity of Burkholderia cepacia lipase in organic solvent but do not significantly affect its conformation.
2005-11-20
Identification of volatile emissions from Platypus mutatus (=sulcatus) (Coleoptera: Platypodidae) and their behavioral activity.
2005-10
Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins.
2005-03
Stereochemical studies of chiral resolving agents, M9PP and H9PP acids.
2004-10
Highly efficient chemical kinetic resolution of bishomoallylic alcohols: synthesis of (R)-sulcatol.
2004-09-16
Manipulating volatile emission in tobacco leaves by expressing Aspergillus nigerbeta-glucosidase in different subcellular compartments.
2004-07
Activity and enantioselectivity of wildtype and lid mutated Candida rugosa lipase isoform 1 in organic solvents.
2004-04-20
Biotransformation of (R)-(+)- and (S)-(-)-citronellol by Aspergillus sp. and Penicillium sp., and the use of solid-phase microextraction for screening.
2004-02-20
Stereochemistry of a diastereoisomeric amphiphile and the species of the lipase influence enzyme activity in the transesterification catalyzed by a lipase-co-lyophilizate with the amphiphile in organic media.
2003-11
Rapid differentiation of new apple cultivars by headspace solid-phase microextraction in combination with chemometrical data processing.
2003-04
[Effects of volatiles from different trophic level on foraging behavior of Aphidius avenae].
2001-08
Novel chemistry of abdominal defensive glands of nymphalid butterfly Agraulis vanillae.
2001-06
Patents

Patents

Name Type Language
SULCATOL
Common Name English
FEMA NO. 4884
Preferred Name English
6-HYDROXY-2-METHYL-2-HEPTENE
Systematic Name English
2-METHYL-2-HEPTEN-6-OL
Systematic Name English
NSC-66273
Code English
6-METHYL-5-HEPTEN-2-OL
Systematic Name English
(±)-6-METHYL-5-HEPTEN-2-OL
Systematic Name English
6-METHYLHEPT-5-EN-2-OL
Systematic Name English
5-HEPTEN-2-OL, 6-METHYL-
Systematic Name English
(±)-SULCATOL
Common Name English
Code System Code Type Description
CHEBI
15833
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
216-377-1
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY
NSC
66273
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY
CAS
1335-09-7
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
NON-SPECIFIC SUBSTITUTION
ALANWOOD
sulcatol
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY
CAS
1569-60-4
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID8051754
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY
FDA UNII
33321H09GI
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY
PUBCHEM
20745
Created by admin on Mon Mar 31 22:51:26 GMT 2025 , Edited by admin on Mon Mar 31 22:51:26 GMT 2025
PRIMARY