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Benzo[b]thiophene-2-carboxaMide, 3-chloro-N-[2-[[(4-fluorophenyl)aMino]carbonyl]-4-Methylphenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216985-39-6

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216985-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216985-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,9,8 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 216985-39:
(8*2)+(7*1)+(6*6)+(5*9)+(4*8)+(3*5)+(2*3)+(1*9)=166
166 % 10 = 6
So 216985-39-6 is a valid CAS Registry Number.

216985-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-N-[2-[(4-fluorophenyl)carbamoyl]-4-methylphenyl]-1-benzothiophene-2-carboxamide

1.2 Other means of identification

Product number -
Other names anthranilamide compound 1

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:216985-39-6 SDS

216985-39-6Downstream Products

216985-39-6Relevant academic research and scientific papers

Neutral inhibitors of the serine protease factor Xa

Shrader, William D.,Young, Wendy B.,Sprengeler, Paul A.,Sangalang, Joan C.,Elrod, Kyle,Carr, Grant

, p. 1801 - 1804 (2001)

A neutral inhibitor of the serine protease factor Xa was identified via a high-throughput screen of a commercial library. The initial lead 1 demonstrated reversible and competitive inhibition kinetics for factor Xa and possessed a high degree of selectivity versus other related serine proteases. Initial modeling efforts and the generation of a series of analogues of 1 are described.

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