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Details

Stereochemistry RACEMIC
Molecular Formula C8H14O
Molecular Weight 126.1962
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-OCTYN-3-OL

SMILES

CCCCCC(O)C#C

InChI

InChIKey=VUGRNZHKYVHZSN-UHFFFAOYSA-N
InChI=1S/C8H14O/c1-3-5-6-7-8(9)4-2/h2,8-9H,3,5-7H2,1H3

HIDE SMILES / InChI

Molecular Formula C8H14O
Molecular Weight 126.1962
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of an enantioselective odorant receptor in the yellow fever mosquito Aedes aegypti.
2009-09-15
Reverse and conventional chemical ecology approaches for the development of oviposition attractants for Culex mosquitoes.
2008-08-22
Evaluation of the enantiomers of 1-octen-3-ol and 1-octyn-3-ol as attractants for mosquitoes associated with a freshwater swamp in Florida, U.S.A.
2007-12
A straightforward synthesis of (-)-phaseolinic acid.
2004-11-12
Novel chemoenzymatic strategy for the synthesis of enantiomerically pure secondary alcohols with sterically similar substituents.
2003-06-27
Practical enantioresolution of alcohols with 2-methoxy-2-(1-naphthyl)propionic acid and determination of their absolute configurations by the (1)H NMR anisotropy method.
2002-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:50:25 GMT 2025
Edited
by admin
on Mon Mar 31 21:50:25 GMT 2025
Record UNII
DG52FEN1K1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(RS)-1-OCTYN-3-OL
Preferred Name English
1-OCTYN-3-OL
Systematic Name English
(±)-1-OCTYN-3-OL
Systematic Name English
1-ETHYNYL-1-HEXANOL
Systematic Name English
3-HYDROXYOCT-1-YNE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
212-455-4
Created by admin on Mon Mar 31 21:50:25 GMT 2025 , Edited by admin on Mon Mar 31 21:50:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID7022124
Created by admin on Mon Mar 31 21:50:25 GMT 2025 , Edited by admin on Mon Mar 31 21:50:25 GMT 2025
PRIMARY
FDA UNII
DG52FEN1K1
Created by admin on Mon Mar 31 21:50:25 GMT 2025 , Edited by admin on Mon Mar 31 21:50:25 GMT 2025
PRIMARY
PUBCHEM
13166
Created by admin on Mon Mar 31 21:50:25 GMT 2025 , Edited by admin on Mon Mar 31 21:50:25 GMT 2025
PRIMARY
CAS
818-72-4
Created by admin on Mon Mar 31 21:50:25 GMT 2025 , Edited by admin on Mon Mar 31 21:50:25 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE