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4-[(1,1,2,2-tetrafluoroethyl)sulfanyl]aniline is an organic compound with the chemical formula C10H10F4NS. It is a derivative of aniline, where a hydrogen atom on the aniline molecule is replaced by a (1,1,2,2-tetrafluoroethyl)sulfanyl group. 4-[(1,1,2,2-tetrafluoroethyl)sulfanyl]aniline is characterized by its fluorinated alkyl chain and sulfanyl functional group, which can contribute to unique chemical properties such as increased lipophilicity and potential reactivity with electrophilic species. It is typically synthesized for use in the development of pharmaceuticals, agrochemicals, or as a building block in the synthesis of more complex organic molecules. The presence of fluorine atoms can significantly alter the physical and chemical properties of the molecule, making it a valuable intermediate in various chemical processes.

713-63-3

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713-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 713-63-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 713-63:
(5*7)+(4*1)+(3*3)+(2*6)+(1*3)=63
63 % 10 = 3
So 713-63-3 is a valid CAS Registry Number.

713-63-3SDS

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 4-(1,1,2,2-tetrafluoroethylsulfanyl)aniline

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:713-63-3 SDS

713-63-3Downstream Products

713-63-3Relevant academic research and scientific papers

Synthesis of Fluoroalkyl Sulfides via Additive-Free Hydrothiolation and Sequential Functionalization Reactions

Sunagawa, Denise E.,Ishida, Naoyoshi,Iwamoto, Hiroaki,Ohashi, Masato,Fruit, Corinne,Ogoshi, Sensuke

, p. 6015 - 6024 (2021/05/04)

A modular synthetic method, involving a hydrothiolation, silylation, and fluoroalkylation, for the construction of highly functionalized fluoroalkyl sulfides has been developed. The use of aprotic polar solvents enables the additive-free chemoselective hydrothiolation of tetrafluoroethylene, trifluorochloroethylene, and hexafluoropropene with various thiols. The stepwise functionalization reactions convert the hydrothiolated intermediates into the tetrafluoroethyl sulfides in high efficiency. The method avoids the use of the environmental pollutant Halon-2402, which was employed as a building block in a reported synthetic route.

3-(p-Alkylsulfonylphenyl)oxazolidinone derivatives as antibacterial agents

-

, (2008/06/13)

This invention relates to novel 3-(p-alkylsulfonylphenyl)oxazolidinone derivatives, pharmaceutical compositions containing them and methods of using them to alleviate bacterial infections in mammals.

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