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2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride, with the chemical formula C7H4Cl2F3O2S, is a highly reactive and corrosive sulfonyl chloride derivative. It features a chlorine atom and a trifluoromethyl group attached to a benzene ring, which makes it a versatile building block for the synthesis of various pharmaceuticals and agrochemicals. Due to its toxic and irritating nature, it requires careful handling and appropriate safety measures.

175205-54-6

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175205-54-6 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride is used as a sulfonylating agent in the synthesis of pharmaceuticals. Its unique chemical structure allows for the creation of a wide range of drug molecules with potential therapeutic applications.
Used in Agrochemical Production:
2-CHLORO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE is also utilized in the production of agrochemicals, where its sulfonylating properties contribute to the development of effective pesticides and other agricultural chemicals.
Used in Dye Manufacturing:
2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride is employed in the manufacturing of dyes, where its chemical reactivity and functional groups enable the production of various colorants for different industries.
Used in Polymer Production:
In the polymer industry, 2-CHLORO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE is used to synthesize polymers with specific properties, such as enhanced stability or reactivity, by incorporating its sulfonyl chloride group into the polymer backbone.
Used in Industrial Chemical Production:
2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride is also used in the production of other industrial chemicals, where its versatile chemical structure and reactivity contribute to the development of novel compounds for various applications.
It is crucial to handle 2-chloro-4-(trifluoromethyl)benzenesulfonyl chloride with care due to its corrosive and toxic nature, ensuring that proper safety measures are in place to protect both the environment and the individuals working with 2-CHLORO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE.

Check Digit Verification of cas no

The CAS Registry Mumber 175205-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,0 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175205-54:
(8*1)+(7*7)+(6*5)+(5*2)+(4*0)+(3*5)+(2*5)+(1*4)=126
126 % 10 = 6
So 175205-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl2F3O2S/c8-5-3-4(7(10,11)12)1-2-6(5)15(9,13)14/h1-3H

175205-54-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L19105)  2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride, 97%   

  • 175205-54-6

  • 1g

  • 946.0CNY

  • Detail
  • Alfa Aesar

  • (L19105)  2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride, 97%   

  • 175205-54-6

  • 5g

  • 3488.0CNY

  • Detail
  • Aldrich

  • (638366)  2-Chloro-4-(trifluoromethyl)benzenesulfonylchloride  97%

  • 175205-54-6

  • 638366-1G

  • 1,353.69CNY

  • Detail
  • Aldrich

  • (638366)  2-Chloro-4-(trifluoromethyl)benzenesulfonylchloride  97%

  • 175205-54-6

  • 638366-5G

  • 4,527.90CNY

  • Detail

175205-54-6SDS

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 2-CHLORO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 2-chloro-4-trifluoromethylphenylsulfonyl 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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:175205-54-6 SDS

175205-54-6Relevant articles and documents

Preparation method of halogenated aromatic sulfonyl chloride

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Paragraph 0040-0058; 0084-0090, (2021/08/14)

The invention discloses a preparation method of halogenated aromatic sulfonyl chloride. The preparation method specifically comprises the following steps of: 1, preparing a SO2 water saturated solution; 2, preparing a heavy ammonium salt; and 3, preparing sulfonyl chloride, finally desolventizing the filtrate at 30-38 DEG C under reduced pressure by using a water pump until no liquid is discharged to obtain 6.0 g of brownish red liquid, controlling the purity to be 93.2% by using HPLC (High Performance Liquid Chromatography), and standing overnight to obtain a solid on the second day. The thionyl chloride used in the method is used as a raw material, the method is economical, cheap and easy to operate, the whole reaction process is safe and stable, the reaction efficiency is high, the pure product rate of the obtained product is high, and industrial large-scale production is easy.

Substituted Disulfonamide Compounds

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Page/Page column 56, (2010/06/22)

Substituted disulfonamide compounds corresponding to formula I: In which R1, R2, R3, R4a, R4b, R5a, R5b, R8, R9a, R9b, R10, R11, a, b, s, t and A have defined meanings, pharmaceutical compositions containing one or more such compounds, processes for preparing such compounds, and a method of using such compounds for the treatment or inhibition of pain and/or other conditions mediated by the bradykinin receptor 1 (BR1).

Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists

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, (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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