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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H18O
Molecular Weight 130.2279
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-OCTANOL, (2R)-

SMILES

CCCCCC[C@@H](C)O

InChI

InChIKey=SJWFXCIHNDVPSH-MRVPVSSYSA-N
InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3/t8-/m1/s1

HIDE SMILES / InChI

Molecular Formula C8H18O
Molecular Weight 130.2279
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Stereocontrolled diels-alder cycloadditions of sugar-derived dihydropyranones with dienes.
2002 Nov 1
Effect of additives on electrokinetic properties of colloidal alumina suspension.
2002 Oct 1
Photoinduced polarization inversion in a ferroelectric liquid crystal using an ambidextrous chiral thioindigo dopant.
2003 Jun 11
On the mechanism of the unexpected facile formation of meso-diacetate products in enzymatic acetylation of alkanediols.
2003 Mar 21
Photoswitching of ferroelectric liquid crystals using chiral thioindigo dopants: The development of a photochemical switch hitter.
2004
Directed metalation route to ferroelectric liquid crystals with a chiral fluorenol core: the effect of restricted rotation on polar order.
2004 Feb 4
The stereoselectivity and catalytic properties of Xanthobacter autotrophicus 2-[(R)-2-Hydroxypropylthio]ethanesulfonate dehydrogenase are controlled by interactions between C-terminal arginine residues and the sulfonate of coenzyme M.
2004 Jun 1
The nature of the hydrophobic n-alkanol binding site within the C1 domains of protein kinase Calpha.
2004 Jun 15
General anesthetic octanol and related compounds activate wild-type and delF508 cystic fibrosis chloride channels.
2004 Mar
A hollow-fiber membrane extraction process for recovery and separation of lactic acid from aqueous solution.
2004 Spring
The effect of transdermal delivery of fentanyl on activity in growing pigs.
2005
Perceptual and neural olfactory similarity in honeybees.
2005 Apr
Studies on the mechanism of Indigo Carmine removal by solvent sublation.
2005 Dec 1
High-yield conversion of (R)-2-octanol from the corresponding racemate by stereoinversion using Candida rugosa.
2005 Jan
Role of histamine as a putative inhibitory transmitter in the honeybee antennal lobe.
2006 Dec 29
Effect of lipase immobilization on resolution of (R, S)-2-octanol in nonaqueous media using modified ultrastable-Y molecular sieve as support.
2006 Jul
Anti-prelog reduction of prochiral carbonyl compounds by Oenococcus oeni in a biphasic system.
2006 Jul
Core-shell type of nanoparticles composed of poly[(n-butyl cyanoacrylate)-co-(2-octyl cyanoacrylate)] copolymers for drug delivery application: synthesis, characterization and in vitro degradation.
2006 Nov 15
Functional characterization of alcohol oxidases from Aspergillus terreus MTCC 6324.
2006 Oct
Comparison of hydrogen bonding in 1-octanol and 2-octanol as probed by spectroscopic techniques.
2006 Sep 14
Hydrogen bonding in liquid and supercritical 1-octanol and 2-octanol assessed by near and midinfrared spectroscopy.
2006 Sep 7
Odor concentration invariance by chemical ratio coding.
2007
Understanding the logics of pheromone processing in the honeybee brain: from labeled-lines to across-fiber patterns.
2007
Determination of alcohol compounds using corona discharge ion mobility spectrometry.
2007
(S)-(+)-2-octanol as a chiral oil core for the microemulsion electrokinetic chromatographic separation of chiral basic drugs.
2007 Sep
Associative and non-associative plasticity in kenyon cells of the honeybee mushroom body.
2008
Deracemization of secondary alcohols through a concurrent tandem biocatalytic oxidation and reduction.
2008
Diastereoselective synthesis of (R)-(alkyl)-beta-D-galactopyranoside by using beta-galactosidase (Aspergillus oryzae) in low-water media.
2008 Jan 1
Activity of essential oils and individual components against acetyl- and butyrylcholinesterase.
2008 Jul-Aug
[Rapid determination of volatile flavor compounds in soy sauce using head space solid-phase microextraction and gas chromatography-mass spectrometry].
2008 May
Retraction: (S)-(+)-2-octanol as a chiral oil core for the microemulsion electrokinetic chromatographic separation of chiral basic drugs [Anal. Sci., Vol. 23, p. 1071 (2007)].
2008 May
Differential odor processing in two olfactory pathways in the honeybee.
2009
Telomerization of butadiene with glycerol: reaction control through process engineering, solvents, and additives.
2009
Optimization of poly(GMA-co-EDMA) monolithic support for trypsin nanoreactor fabrication.
2009 Jul
Intelligent chiral sensing based on supramolecular and interfacial concepts.
2010
Chromatography-olfactometry study of the aroma of fino sherry wines.
2010
Purification and characterization of an anti-Prelog alcohol dehydrogenase from Oenococcus oeni that reduces 2-octanone to (R)-2-octanol.
2010 Apr
Solvent free oxidation of primary alcohols and diols using thymine iron(III) catalyst.
2010 Dec 28
Calcium imaging in the ant Camponotus fellah reveals a conserved odour-similarity space in insects and mammals.
2010 Feb 26
Spontaneous product segregation from reactions in ionic liquids: application in Pd-catalyzed aliphatic alcohol oxidation.
2010 Feb 28
Energy transfer from silica core-surfactant shell nanoparticles to hosted molecular fluorophores.
2010 Nov 18
Effects of T-type calcium channel blockers on cocaine-induced hyperlocomotion and thalamocortical GABAergic abnormalities in mice.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:52:32 GMT 2023
Edited
by admin
on Fri Dec 15 17:52:32 GMT 2023
Record UNII
2SHB67XF6H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-OCTANOL, (2R)-
Systematic Name English
L-(-)-OCTAN-2-OL
Common Name English
(-)-2-OCTANOL
Systematic Name English
(R)-(-)-2-OCTYL ALCOHOL
Systematic Name English
(2R)-2-OCTANOL
Systematic Name English
(R)-1-METHYLHEPTANOL
Systematic Name English
2-OCTANOL L-FORM [MI]
Common Name English
(R)-(-)-2-OCTANOL
Systematic Name English
2-OCTANOL, L-
Common Name English
2-OCTANOL, (R)-
Systematic Name English
2-OCTANOL, (THETA)-
Common Name English
L-2-OCTANOL
Common Name English
2-OCTANOL L-FORM
MI  
Common Name English
(R)-2-OCTANOL
Systematic Name English
Code System Code Type Description
CHEBI
37871
Created by admin on Fri Dec 15 17:52:32 GMT 2023 , Edited by admin on Fri Dec 15 17:52:32 GMT 2023
PRIMARY
PUBCHEM
80080
Created by admin on Fri Dec 15 17:52:32 GMT 2023 , Edited by admin on Fri Dec 15 17:52:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-777-0
Created by admin on Fri Dec 15 17:52:32 GMT 2023 , Edited by admin on Fri Dec 15 17:52:32 GMT 2023
PRIMARY
FDA UNII
2SHB67XF6H
Created by admin on Fri Dec 15 17:52:32 GMT 2023 , Edited by admin on Fri Dec 15 17:52:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID80884209
Created by admin on Fri Dec 15 17:52:32 GMT 2023 , Edited by admin on Fri Dec 15 17:52:32 GMT 2023
PRIMARY
CAS
5978-70-1
Created by admin on Fri Dec 15 17:52:32 GMT 2023 , Edited by admin on Fri Dec 15 17:52:32 GMT 2023
PRIMARY
MERCK INDEX
m8111
Created by admin on Fri Dec 15 17:52:32 GMT 2023 , Edited by admin on Fri Dec 15 17:52:32 GMT 2023
PRIMARY Merck Index