Merck
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147982

Sigma-Aldrich

(S)-(+)-2-Octanol

99%

Fórmula linear:
CH3(CH2)5CH(OH)CH3
Número CAS:
Peso molecular:
130.23
Beilstein:
1719323
Número EC:
Número MDL:
ID de substância PubChem:

Nível de qualidade

100

teor

99%

forma

liquid

atividade óptica

[α]20/D +9.5°, neat

pureza óptica

ee: 98% (GLC)

índice de refração

n20/D 1.426 (lit.)

pb

175 °C (lit.)

densidade

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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Aplicação

(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.

Embalagem

5 g in glass bottle

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2

Código de classe de armazenamento

10 - Combustible liquids

WGK

WGK 3

Ponto de fulgor (ºF)

168.8 °F

Ponto de fulgor (ºC)

76 °C

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificado de análise

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Certificado de origem

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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)
Development of simulation approach for two-dimensional chiral molecular self-assembly driven by hydrogen bond at the liquid/solid interface
Qin Y, et al.
Surface Science, 663, 71-80 (2017)
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)
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

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