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About This Item
Linear Formula:
CH3(CH2)5CH(OH)CH3
CAS Number:
Molecular Weight:
130.23
Beilstein:
1719323
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
liquid
optical activity
[α]20/D +9.5°, neat
optical purity
ee: 98% (GLC)
refractive index
n20/D 1.426 (lit.)
bp
175 °C (lit.)
density
0.822 g/mL at 25 °C (lit.)
SMILES string
CCCCCC[C@H](C)O
InChI
1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3/t8-/m0/s1
InChI key
SJWFXCIHNDVPSH-QMMMGPOBSA-N
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Application
(S)-(+)-2-Octanol can be used:
- To prepare the solution of 5-(benzyloxy)-isophthalic acid derivative, which is used as a 2D chiral self-assembly system comprising pyrolytic graphite.
- As a chiral template in the study of enantioselective glycidol esterification.
- As a starting material for the preparation of (+)-(S)-2-octyI tosylate, an intermediate used to prepare (−)-(R)-2-halo and azido octanes.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
168.8 °F - closed cup
Flash Point(C)
76 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Convenient preparation of optically active 2-halooctanes and related compounds
San Filippo Jr J and Romano LJ
The Journal of Organic Chemistry, 40(10), 1514-1515 (1975)
Xiao-Yang Ou et al.
Journal of biotechnology, 299, 37-43 (2019-05-03)
Highly efficient asymmetric reduction of 2-octanone to (R)-2-octanol catalyzed by immobilized Acetobacter sp. CCTCC M209061 cells was achieved in a biphasic system. Bioreduction conducted in aqueous single phase buffer was limited due to poor solubility and toxicity towards cells cause
Paul Masset et al.
Cell, 182(1), 112-126 (2020-06-07)
Every decision we make is accompanied by a sense of confidence about its likely outcome. This sense informs subsequent behavior, such as investing more-whether time, effort, or money-when reward is more certain. A neural representation of confidence should originate from
Effect of imprinting sol-gel immobilized lipase with chiral template substrates in esterification of (R)-(+)-and (S)-(-)-glycidol.
Furukawa S, et al.
Journal of Molecular Catalysis. B, Enzymatic, 17(1), 23-28 (2002)
Francesca Palombo et al.
The journal of physical chemistry. B, 110(36), 18017-18025 (2006-09-08)
Liquid 1-octanol and 2-octanol have been investigated by infrared (IR), Raman, and Brillouin experiments in the 10-90 degrees C temperature range. Self-association properties of the neat liquids are described in terms of a three-state model in which OH oscillators differently
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