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(R)-(−)-2-Octanol

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For Research Use Only | Not For Clinical Use
CATAP5978701
CAS5978-70-1
MDL NumberMFCD00064284
Molecular Weight130.23
EC Number227-777-0
InChI KeySJWFXCIHNDVPSH-MRVPVSSYSA-N
REAXYS Number1719324
Descriptionfor chiral derivatization, 99%
Density0.820 g/mL at 20 °C (lit.)
Assay99%
BP175 °C (lit.)
Gradefor chiral derivatization
Linear FormulaCH3(CH2)5CH(OH)CH3
Refractive Indexn20/D 1.426 (lit.)
Size5G, 10G
1

High-yield Conversion of (R)-2-octanol From the Corresponding Racemate by Stereoinversion Using Candida Rugosa

Yao Nie, Yan Xu, Xiao Qing Mu, Yan Tang, Juan Jiang, Zhi Hao Sun

Biotechnol Lett. 2005 Jan;27(1):23-6.

PMID: 15685415

1

Inversion of Substrate Stereoselectivity of Horse Liver Alcohol Dehydrogenase by Substitutions of Ser-48 and Phe-93

Keehyuk Kim, Bryce V Plapp

Chem Biol Interact. 2017 Oct 1;276:77-87.

PMID: 28025168

1

Novel Chiral Tool, (R)-2-octanol Dehydrogenase, From Pichia Finlandica: Purification, Gene Cloning, and Application for Optically Active α-haloalcohols

Hiroaki Yamamoto, Masatake Kudoh

Appl Microbiol Biotechnol. 2013 Sep;97(18):8087-96.

PMID: 23274959

1

Novel Magnetic Cross-Linked Lipase Aggregates for Improving the Resolution of (R, S)-2-octanol

Ying Liu, Chen Guo, Chun-Zhao Liu

Chirality. 2015 Mar;27(3):199-204.

PMID: 25482205

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