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4-FLUORO-2-METHYLBENZENESULFONYL CHLORIDE is a chemical compound with the molecular formula C7H6ClFO2S. It is a sulfonamide derivative that is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical products and drug intermediates. This white to off-white solid has a melting point of 46-49 °C and is known for its reactivity with amines and alcohols, forming sulfonamides and sulfonates, respectively.

7079-48-3

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7079-48-3 Usage

Uses

Used in Pharmaceutical Industry:
4-FLUORO-2-METHYLBENZENESULFONYL CHLORIDE is used as a building block for the synthesis of pharmaceutical products and drug intermediates due to its reactivity and structural properties that facilitate the creation of diverse medicinal compounds.
Used in Organic Synthesis:
4-FLUORO-2-METHYLBENZENESULFONYL CHLORIDE is used as a reagent in organic synthesis for its ability to react with amines and alcohols to form sulfonamides and sulfonates, which are important in the development of various organic compounds.
Used in Agrochemical Production:
4-FLUORO-2-METHYLBENZENESULFONYL CHLORIDE is used as an intermediate in the production of agrochemicals, contributing to the development of effective compounds for agricultural applications.
Used in Veterinary Drug Manufacturing:
4-FLUORO-2-METHYLBENZENESULFONYL CHLORIDE is also utilized as an intermediate in the manufacturing of veterinary drugs, playing a role in the creation of medications for animal health.

Check Digit Verification of cas no

The CAS Registry Mumber 7079-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7079-48:
(6*7)+(5*0)+(4*7)+(3*9)+(2*4)+(1*8)=113
113 % 10 = 3
So 7079-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClFO2S/c1-5-4-6(9)2-3-7(5)12(8,10)11/h2-4H,1H3

7079-48-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L19517)  4-Fluoro-2-methylbenzenesulfonyl chloride, 97%   

  • 7079-48-3

  • 1g

  • 367.0CNY

  • Detail
  • Alfa Aesar

  • (L19517)  4-Fluoro-2-methylbenzenesulfonyl chloride, 97%   

  • 7079-48-3

  • 5g

  • 1481.0CNY

  • Detail
  • Aldrich

  • (558567)  4-Fluoro-2-methylbenzenesulfonylchloride  97%

  • 7079-48-3

  • 558567-1G

  • 336.96CNY

  • Detail
  • Aldrich

  • (558567)  4-Fluoro-2-methylbenzenesulfonylchloride  97%

  • 7079-48-3

  • 558567-5G

  • 1,217.97CNY

  • Detail

7079-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-2-methylbenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 4-FLUORO-2-METHYLBENZENESULFONYL 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:7079-48-3 SDS

7079-48-3Upstream product

7079-48-3Relevant articles and documents

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.

Synthesis of fused sulfonamide (1,1-dioxoisothiazole)substituted 1,5-diarylpyrazoles as cyclooxygenase inhibitors

Pal, Manojit,Veeramaneni, Venugopal Rao,Kumar, Sanjeev,Lohray, Vidya B.,Yeleswarapu, Koteswar Rao

, p. 1095 - 1101 (2007/10/03)

First synthesis of novel 1,1-dioxo-2,3-dihydrobenzo[d] isothiazolyl substituted 1,5-diarylpyrazoles has been accomplished via oxidative cyclization of 4-fluoro-2-methyl benzenesulfonamide followed by the treatment with hydrazine and then with 1,3-dicarbon

Synthesis and cyclooxygenase-2 inhibiting property of 1,5-diarylpyrazoles with substituted benzenesulfonamide moiety as pharmacophore: Preparation of sodium salt for injectable formulation

Pal, Manojit,Madan, Manjula,Padakanti, Srinivas,Pattabiraman, Vijaya R.,Kalleda, Srinivas,Vanguri, Akhila,Mullangi, Ramesh,Mamidi, N. V. S. Rao,Casturi, Seshagiri R.,Malde, Alpeshkumar,Gopalakrishnan,Yeleswarapu, Koteswar R.

, p. 3975 - 3984 (2007/10/03)

A series of 1,5-diarylpyrazoles having a substituted benzenesulfonamide moiety as pharmacophore was synthesized and evaluated for cyclooxygenase (COX-1/COX-2) inhibitory activities. Through SAR and molecular modeling, it was found that fluorine substituti

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