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139244-46-5

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139244-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139244-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,4 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139244-46:
(8*1)+(7*3)+(6*9)+(5*2)+(4*4)+(3*4)+(2*4)+(1*6)=135
135 % 10 = 5
So 139244-46-5 is a valid CAS Registry Number.

139244-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoroethyl pyrazine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-pyrazinecarboxylic acid 2,2,2-trifluoroethyl ester

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:139244-46-5 SDS

139244-46-5Downstream Products

139244-46-5Relevant articles and documents

Regioselective enzymatic acylation as a tool for producing solution- phase combinatorial libraries

Mozhaev, Vadim V.,Budde, Cheryl L.,Rich, Joseph O.,Usyatinsky, Alexander Ya.,Michels, Peter C.,Khmelnitsky, Yuri L.,Clark, Douglas S.,Dordick, Jonathan S.

, p. 3971 - 3982 (1998)

A simple combinatorial strategy for sequential regioselective enzymatic acylation of multifunctional lead compounds has been developed and demonstrated using a polyhydroxylated flavonoid, bergenin, as a model. The approach is based on the ability of different enzymes to regioselectively acylate different sizes on a lead molecule without affecting other similar functional groups. In sharp contrast to enzymatic acylation, conventional chemical acylation methods showed almost complete lack of regioselectivity. The enzymatic strategy was applied successfully to produce a solution phase combinatorial library of 167 distinct selectively acylated derivatives of bergenin on a robotic workstation in a 96-well plate format. General applicability of the automated combinatorial biocatalysis strategy is discussed.

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