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771477-12-4

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771477-12-4 Usage

General Description

N-[4-[(4-Amino-2-fluorophenyl)thio]phenyl]acetamide is a chemical compound with the molecular formula C14H12N2O2S. It is an acetamide derivative with a thioether and amino-substituted phenyl group. N-[4-[(4-Amino-2-fluorophenyl)thio]phenyl]acetamide is commonly used in pharmaceutical research as a chemical intermediate or as a building block in the synthesis of various pharmaceutical compounds. It may also have potential biological activities, although further research is needed to fully understand its properties and mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 771477-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,1,4,7 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 771477-12:
(8*7)+(7*7)+(6*1)+(5*4)+(4*7)+(3*7)+(2*1)+(1*2)=184
184 % 10 = 4
So 771477-12-4 is a valid CAS Registry Number.

771477-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(4-amino-2-fluorophenyl)sulfanylphenyl]acetamide

1.2 Other means of identification

Product number -
Other names N-[4-[(4-Amino-2-fluorophenyl)thio]phenyl]acetamide

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

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More Details:771477-12-4 SDS

771477-12-4Relevant articles and documents

Synthesis and antibacterial activity of some aryloxy/thioaryloxy oxazolidinone derivatives

Arora, Vishal,Salunkhe, Manikrao M.,Sinha, Neelima,Sinha, Rakesh K.,Jain, Sanjay

, p. 4647 - 4650 (2007/10/03)

A series of aryloxy/thioaryloxy oxazolidinones has been synthesized and their antibacterial activity in vitro were evaluated and compared with linezolid. A series of aryloxy/thioaryloxy oxazolidinone derivatives has been synthesized and tested for in vitro antibacterial activity by MIC determination against a panel of susceptible and resistant Gram-positive and Gram-negative microorganisms, some of which are resistant to methicillin and vancomycin. Compounds 12a, 12b, 14a, and 14b from this series were found to be equipotent or more potent than linezolid in vitro.

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