Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

346217

Sigma-Aldrich

(R)-(+)-1-(2-Naphthyl)ethanol

98%

Synonym(s):

(R)-(+)-α-Methyl-2-naphthalenemethanol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C10H7CH(CH3)OH
CAS Number:
52193-85-8
Molecular Weight:
172.22
Beilstein:
3195952
MDL number:
MFCD00075344
UNSPSC Code:
12352005
PubChem Substance ID:
24861381
NACRES:
NA.22

Assay

98%

optical activity

[α]20/D +38°, c = 5 in ethanol

mp

68-70 °C (lit.)

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-/m1/s1

InChI key

AXRKCRWZRKETCK-SECBINFHSA-N

Gene Information

human ... UGT2B17(7367) , UGT2B7(7364)

Looking for similar products? Visit Product Comparison Guide

Application

(R)-(+)-1-(2-Naphthyl)ethanol may be used to synthesize (S)-2-chloro-1-phenylethanol by reacting with 2-chloroacetophenone in the presence of a chiral bidentate titanium Lewis acid catalyst.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Bidentate Lewis acids for organic synthesis.
Maruoka K.
Catalysis Today, 66(1), 33-45 (2001)
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service