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3-(Trifluoromethoxy)benzenesulfonyl chloride is a chemical compound with the molecular formula C7H4ClF3O3S. It is a sulfonyl chloride derivative of trifluoromethylphenol, characterized by its strong electrophilic properties. 3-(Trifluoromethoxy)benzenesulfonyl chloride is a key intermediate in the synthesis of various functionalized sulfonyl compounds and is widely used in organic chemistry due to its ability to introduce the trifluoromethoxy functional group into organic molecules, making it a versatile building block.

220227-84-9

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220227-84-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(Trifluoromethoxy)benzenesulfonyl chloride is used as a reagent in the synthesis of pharmaceuticals for its ability to introduce the trifluoromethoxy functional group, which can enhance the pharmacological properties of drug molecules.
Used in Agrochemical Industry:
In the agrochemical industry, 3-(Trifluoromethoxy)benzenesulfonyl chloride is utilized as a reagent in the production of agrochemicals, where its strong electrophilic nature aids in the synthesis of various agrochemical compounds.
Used in Organic Synthesis:
3-(Trifluoromethoxy)benzenesulfonyl chloride is used as a key intermediate in the preparation of various functionalized sulfonyl compounds, playing a crucial role in chemical transformations and the development of new organic compounds.
Used in Chemical Research:
As a strong electrophile, 3-(Trifluoromethoxy)benzenesulfonyl chloride is employed in chemical research to explore its reactivity and potential applications in the synthesis of novel organic molecules and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 220227-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,2 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 220227-84:
(8*2)+(7*2)+(6*0)+(5*2)+(4*2)+(3*7)+(2*8)+(1*4)=89
89 % 10 = 9
So 220227-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClF3O3S/c8-15(12,13)6-3-1-2-5(4-6)14-7(9,10)11/h1-4H

220227-84-9 Well-known Company Product Price

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  • Aldrich

  • (579505)  3-(Trifluoromethoxy)benzenesulfonylchloride  97%

  • 220227-84-9

  • 579505-1G

  • 1,366.56CNY

  • Detail

220227-84-9SDS

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 3-(trifluoromethoxy)benzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 3-(Trifluoromethoxy)benzenesulfonyl chloride

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:220227-84-9 SDS

220227-84-9Relevant academic research and scientific papers

Synthesis of aryl sulfonamides via palladium-catalyzed chlorosulfonylation of arylboronic acids

Debergh, J. Robb,Niljianskul, Nootaree,Buchwald, Stephen L.

supporting information, p. 10638 - 10641 (2013/08/23)

A palladium-catalyzed method for the preparation of sulfonamides is described. The process exhibits significant functional group tolerance and allows for the preparation of a number of arylsulfonyl chlorides and sulfonamides under mild conditions.

Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists

-

, (2008/06/13)

The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.

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