70693
(S)-(−)-1-(1-Naphthyl)ethanol
puriss., ≥99.0% (sum of enantiomers, GC)
Synonym(s):
(S)-(−)-α-Methyl-1-naphthalenemethanol
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About This Item
Empirical Formula (Hill Notation):
C12H12O
CAS Number:
Molecular Weight:
172.22
PubChem Substance ID:
UNSPSC Code:
12352005
Beilstein/REAXYS Number:
2045009
MDL number:
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
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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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