2-OCTANOL, (2S)-

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 Search

SMILES

CCCCCC[C@H](C)O

InChI

InChIKey=SJWFXCIHNDVPSH-QMMMGPOBSA-N

InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3/t8-/m0/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

Title	Date	PubMed
Asymmetric reduction of ketones with catecholborane using 2,6-BODOL complexes of titanium(IV) as catalysts.	2001 May 18	11411988
On the mechanism of the unexpected facile formation of meso-diacetate products in enzymatic acetylation of alkanediols.	2003 Mar 21	12636384
Regio- and enantioselective alkane hydroxylation with engineered cytochromes P450 BM-3.	2003 Nov 5	14583039
Directed metalation route to ferroelectric liquid crystals with a chiral fluorenol core: the effect of restricted rotation on polar order.	2004 Feb 4	14746485
Perceptual and neural olfactory similarity in honeybees.	2005 Apr	15736975
High-yield conversion of (R)-2-octanol from the corresponding racemate by stereoinversion using Candida rugosa.	2005 Jan	15685415
Anti-prelog reduction of prochiral carbonyl compounds by Oenococcus oeni in a biphasic system.	2006 Jul	16794770
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	16857330
Comparison of hydrogen bonding in 1-octanol and 2-octanol as probed by spectroscopic techniques.	2006 Sep 14	16956293
Deracemization of secondary alcohols through a concurrent tandem biocatalytic oxidation and reduction.	2008	18072189
Diastereoselective synthesis of (R)-(alkyl)-beta-D-galactopyranoside by using beta-galactosidase (Aspergillus oryzae) in low-water media.	2008 Jan 1	18024031
Activity of essential oils and individual components against acetyl- and butyrylcholinesterase.	2008 Jul-Aug	18810999
Differential odor processing in two olfactory pathways in the honeybee.	2009	20198105
Purification and characterization of an anti-Prelog alcohol dehydrogenase from Oenococcus oeni that reduces 2-octanone to (R)-2-octanol.	2010 Apr	20035369
Solvent free oxidation of primary alcohols and diols using thymine iron(III) catalyst.	2010 Dec 28	21042629
Calcium imaging in the ant Camponotus fellah reveals a conserved odour-similarity space in insects and mammals.	2010 Feb 26	20187931
Effects of T-type calcium channel blockers on cocaine-induced hyperlocomotion and thalamocortical GABAergic abnormalities in mice.	2010 Oct	20652540

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:45:24 GMT 2023` Edited by `admin` on `Fri Dec 15 17:45:24 GMT 2023`
Record UNII	2855UV552L
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

2-OCTANOL, (2S)-

Systematic Name

English

2-OCTANOL, D-

Common Name

English

2-OCTANOL, (S)-

Systematic Name

English

(S)-(+)-2-OCTYL ALCOHOL

Systematic Name

English

(S)-2-OCTANOL

Systematic Name

English

(2S)-OCTANOL

Common Name

English

(S)-1-METHYLHEPTYL ALCOHOL

Systematic Name

English

(S)-(+)-2-OCTANOL

Systematic Name

English

(S)-2-OCTYL ALCOHOL

Systematic Name

English

2-OCTANOL D-FORM [MI]

Common Name

English

D-(+)-OCTAN-2-OL

Common Name

English

(2S)-2-OCTANOL

Systematic Name

English

2-OCTANOL, (S)-(+)-

Systematic Name

English

D-2-OCTANOL

Common Name

English

(+)-2-OCTANOL

Systematic Name

English

2-OCTANOL D-FORM

Common Name

English

Code System Code Type Description

ECHA (EC/EINECS)

228-213-6