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159383-84-3

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159383-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159383-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,3,8 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 159383-84:
(8*1)+(7*5)+(6*9)+(5*3)+(4*8)+(3*3)+(2*8)+(1*4)=173
173 % 10 = 3
So 159383-84-3 is a valid CAS Registry Number.

159383-84-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3,3,3-trifluoro-2-phenylpropane-1,2-diol

1.2 Other means of identification

Product number -
Other names (R)-3,3,3-trifluoro-2-phenylpropane-1,2-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:159383-84-3 SDS

159383-84-3Relevant articles and documents

A short route to a Mosher's acid precursor via catalytic asymmetric dihydroxylation (AD)

Bennani,Vanhessche,Sharpless

, p. 1473 - 1476 (1994)

α-Methoxy-α-(trifluoromethyl)phenyl acetic acid (MTPA) is a valuable derivatizing agent for enantiomeric excess determination of alcohols and amines. A short synthesis of a precursor to this compound, based on the asymmetric dihydroxylation (AD) reaction

Enantioselective synthesis of arylmethoxyacetic acid derivatives

Moreno-Dorado, F. Javier,Guerra, Francisco M.,Ortega, Maria J.,Zubia, Eva,Massanet, Guillermo M.

, p. 503 - 510 (2007/10/03)

The preparation of several arylmethoxyacetic acids by a sequence of asymmetric dihydroxylation and further oxidation of the resulting glycol with TEMPO/NaClO/NaClO2 is described. The scope and limitations of the reaction are discussed.

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