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N-{2-[(methylsulfonyl)amino]-5-(trifluoromethyl)pyridin-3-yl}cyclohex-3-ene-1-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141284-08-4

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141284-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141284-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141284-08:
(8*1)+(7*4)+(6*1)+(5*2)+(4*8)+(3*4)+(2*0)+(1*8)=104
104 % 10 = 4
So 141284-08-4 is a valid CAS Registry Number.

141284-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(methanesulfonamido)-5-(trifluoromethyl)pyridin-3-yl]cyclohex-3-ene-1-carboxamide

1.2 Other means of identification

Product number -
Other names 3-Cyclohexene-1-carboxamide,N-(2-((methylsulfonyl)amino)-5-(trifluoromethyl)-3-pyridinyl)

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:141284-08-4 SDS

141284-08-4Downstream Products

141284-08-4Relevant academic research and scientific papers

Synthesis and antipancreatitis activities of novel N-(2-sulfonylamino-5- trifluoromethyl-3-pyridyl)carboxamide derivatives as phospholipase A2 inhibitors

Kimura,Yotsuya,Yuki,Sugi,Shigehara,Haga

, p. 1696 - 1700 (1995)

Novel N-(2-sulfonylamino-5-trifluoromethyl-3-pyridyl)carboxamide derivatives have been prepared and evaluated as phospholipase A2 (PLA2) inhibitors. Among these compounds, IS-741 (sodium salt of 1j), which showed the highest and the most stable therapeutic effect on acute hemorrhagic pancreatitis induced by the closed duodenal loop method in rats, was selected as a candidate for further development.

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