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70693

(S)-(-)-1-(1-萘基)乙醇

Name: (<I>S</I>)-(-)-1-(1-萘基)乙醇
Brand: SIAL

puriss., ≥99.0% (sum of enantiomers, GC)

别名:

(S)-(-)-α-甲基-1-萘甲醇

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关于此项目

经验公式（希尔记法）:

C₁₂H₁₂O

化学文摘社编号:

15914-84-8

分子量:

172.22

PubChem Substance ID:

329762677

UNSPSC Code:

12352005

Beilstein/REAXYS Number:

2045009

MDL number:

MFCD00077831

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grade

puriss.

assay

≥99.0% (sum of enantiomers, GC)

optical activity

[α]20/D −78±2°, c = 1% in methanol

optical purity

enantiomeric ratio: ≥99:1 (HPLC)

mp

45-47.5 °C

SMILES string

C[C@H](O)c1cccc2ccccc12

InChI

1S/C12H12O/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9,13H,1H3/t9-/m0/s1

InChI key

CDRQOYRPWJULJN-VIFPVBQESA-N

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

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Stereochemical sensitivity of the human UDP-glucuronosyltransferases 2B7 and 2B17.

Ingo Bichlmaier et al.

Journal of medicinal chemistry, 49(5), 1818-1827 (2006-03-03)

A set of 28 enantiomers comprising rigid and flexible secondary alcohols was synthesized by the asymmetric Corey-Bakshi-Shibata reduction. The enantiomerically pure alcohols were subjected to enzymatic glucuronidation assays employing the human UDP-glucuronosyltransferases (UGTs) 2B7 and 2B17. Both UGTs displayed high

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