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2-Thiopheneacetic acid, 5-(4-fluorophenyl)-4-[4-(methylsulfonyl)phenyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140402-47-7

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140402-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140402-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,4,0 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140402-47:
(8*1)+(7*4)+(6*0)+(5*4)+(4*0)+(3*2)+(2*4)+(1*7)=77
77 % 10 = 7
So 140402-47-7 is a valid CAS Registry Number.

140402-47-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-(4-fluorophenyl)-4-[4-(methylsulfonyl)phenyl]thiophene-2-acetate

1.2 Other means of identification

Product number -
Other names [5-(4-Fluoro-phenyl)-4-(4-methanesulfonyl-phenyl)-thiophen-2-yl]-acetic acid methyl 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:140402-47-7 SDS

140402-47-7Relevant academic research and scientific papers

Studies on anti-inflammatory agents. VI. Synthesis and pharmacological properties of 2,3-diarylthiophenes

Tsuji, Kiyoshi,Nakamura, Katsuya,Ogino, Takashi,Konishi, Nobukiyo,Tojo, Takashi,Ochi, Takehiro,Seki, Nobuo,Matsuo, Masaaki

, p. 279 - 286 (2007/10/03)

A series of novel 5-substituted-2,3-diarylthiophenes has been synthesized and found to be active in the rat adjuvant arthritis (AA) model and/or in the yeast-induced hyperalgesia (Randall-Selitto) assay. Among the compounds synthesized herein, 2-(4-fluorophenyl)-3-[4- (methylsulfonyl)phenyl]-S-(trifluoromethyl)thiophene (6a) exhibited the most potent activities on AA, collagen-Induced arthritis (CIA) and the delayed- type hypersensitivity response to type II collagen. 5-Bromo-2-[4- (methylamino)phenyl]-3-[4-(methylsulfinyl)phenyl]thiophene (38) is also a potent inhibitor of AA, CIA, hyperalgesia and in vitro tumor necrosis factor- α production.

Thiophene derivatives

-

, (2008/06/13)

This invention relates to new thiophene derivatives having antiinflammatory and analgesic activities and represented by the general formula [I]: STR1 wherein R1 is hydrogen, halogen, cyano, substituted lower alkyl, substituted or unsubstituted

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