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243967-42-2

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243967-42-2 Usage

Biological Activity

Selective inhibitor of protein-tyrosine phosphatase 1B (PTP1B) (K i values are 0.29, 59, 560, 1100, > 2000, > 2000 and > 2000 μ M for PTP1B, CD45 D1D2, PTP β , PTP ε D1, SHP-1, PTP α D1 and LAR D1D2 respectively).

Check Digit Verification of cas no

The CAS Registry Mumber 243967-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,9,6 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 243967-42:
(8*2)+(7*4)+(6*3)+(5*9)+(4*6)+(3*7)+(2*4)+(1*2)=162
162 % 10 = 2
So 243967-42-2 is a valid CAS Registry Number.

243967-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name TCS 401,2-[(Carboxycarbonyl)amino]-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylicacidhydrochloride

1.2 Other means of identification

Product number -
Other names TCS 401

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:243967-42-2 SDS

243967-42-2Downstream Products

243967-42-2Relevant articles and documents

Synthesis of tetrasubstituted thiophenes on solid-support using the Gewald reaction

Castanedo, Georgette M.,Sutherlin, Daniel P.

, p. 7181 - 7184 (2001)

The Gewald reaction was performed on solid support. This reaction combines a ketone or aldehyde, an activated nitrile, and sulfur in the presence of a suitable amine base to make tri- and tetrasubstituted thiophenes. After optimizing conditions for maximum yield and purity, the scope of the reaction was investigated. Finally, this method is highlighted in the synthesis of two biologically relevant compounds.

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