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49584-26-1

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49584-26-1 Usage

Chemical Properties

Light orange solid

Check Digit Verification of cas no

The CAS Registry Mumber 49584-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,8 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 49584-26:
(7*4)+(6*9)+(5*5)+(4*8)+(3*4)+(2*2)+(1*6)=161
161 % 10 = 1
So 49584-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClNO2S/c8-12(10,11)7-3-1-6(5-9)2-4-7/h1-4H

49584-26-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A14081)  4-Cyanobenzenesulfonyl chloride, 97%   

  • 49584-26-1

  • 1g

  • 686.0CNY

  • Detail
  • Alfa Aesar

  • (A14081)  4-Cyanobenzenesulfonyl chloride, 97%   

  • 49584-26-1

  • 5g

  • 2415.0CNY

  • Detail
  • Alfa Aesar

  • (A14081)  4-Cyanobenzenesulfonyl chloride, 97%   

  • 49584-26-1

  • 25g

  • 10222.0CNY

  • Detail
  • Aldrich

  • (638331)  4-Cyanobenzenesulfonylchloride  97%

  • 49584-26-1

  • 638331-1G

  • 773.37CNY

  • Detail
  • Aldrich

  • (638331)  4-Cyanobenzenesulfonylchloride  97%

  • 49584-26-1

  • 638331-5G

  • 2,688.66CNY

  • Detail

49584-26-1Relevant articles and documents

HETEROCYCLIC COMPOUNDS WITH AN ROR(GAMMA)T MODULATING ACTIVITY

-

Paragraph 0605, (2018/03/06)

The present invention relates to a compound that may have an ROR(gamma)t modulating activity and can thus be useful in the treatment of cancer.

Aminoxidation of Arenethiols to N-Chloro-N-sulfonyl Sulfinamides

Yang, Zhanhui,Xu, Wei,Wu, Qiuyue,Xu, Jiaxi

, p. 3051 - 3057 (2016/04/26)

A simple and efficient method to synthesize N-chloro-N-sulfonylsulfinamides by the direct aminoxidation of arenethiols under aqueous and mild conditions is disclosed, geminally installing the oxo and amino groups on the sulfur atom of arenethiols. The products have been primarily developed as sulfinylation reagents to convert Grignard reagents into sulfoxides, and as amination reagents to convert secondary amines into hydrazine derivatives.

Aqueous process chemistry: The preparation of aryl sulfonyl chlorides

Hogan, Philip J.,Cox, Brian G.

experimental part, p. 875 - 879 (2010/04/22)

The use of aqueous acidic conditions for the preparation of arylsulfonyl chlorides from diazonium salts in the presence of copper salts, preferably CuCl, together with thionyl chloride as the sulfur dioxide source, has considerable advantages over recommended literature procedures, whereby reactions are carried out in acetic acid with minimisation of water content of the solvent. The method has been shown to be successful for a wide range of electron-deficient and electron-neutral aryl substrates. The sulfonyl chlorides are protected from hydrolysis by their low solubility in water, which results in their direct precipitation from the reaction mixture in good yields (>70%) and high strength (>98% w/w). The aqueous process, which is additionally safer and more robust, can be readily scaled up and has significant environmental benefits.

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