323144
(S)-(−)-α−Methyl-2-naphthalenemethanol
98%
Synonym(s):
(S)-(−)-1-(2-Naphthyl)ethanol
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Assay
98%
optical activity
[α]20/D −40°, c = 5 in ethanol
mp
70-71 °C (lit.)
functional group
hydroxyl
SMILES string
C[C@H](O)c1ccc2ccccc2c1
InChI
1S/C12H12O/c1-9(13)11-7-6-10-4-2-3-5-12(10)8-11/h2-9,13H,1H3/t9-/m0/s1
InChI key
AXRKCRWZRKETCK-VIFPVBQESA-N
Gene Information
human ... UGT2B17(7367) , UGT2B7(7364)
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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