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37526-59-3

37526-59-3

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37526-59-3 Usage

Uses

2-(Trifluoromethoxy)benzenesulfonamide can be used to treat cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 37526-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,2 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37526-59:
(7*3)+(6*7)+(5*5)+(4*2)+(3*6)+(2*5)+(1*9)=133
133 % 10 = 3
So 37526-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3NO3S/c8-7(9,10)14-5-3-1-2-4-6(5)15(11,12)13/h1-4H,(H2,11,12,13)

37526-59-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail

  • TCI America

  • (T2604)  2-(Trifluoromethoxy)benzenesulfonamide  >98.0%(GC)(T)

  • 37526-59-3

  • 5g

  • 490.00CNY

  • Detail

  • TCI America

  • (T2604)  2-(Trifluoromethoxy)benzenesulfonamide  >98.0%(GC)(T)

  • 37526-59-3

  • 25g

  • 1,590.00CNY

  • Detail

  • Alfa Aesar

  • (B21609)  2-(Trifluoromethoxy)benzenesulfonamide, 99%   

  • 37526-59-3

  • 1g

  • 655.0CNY

  • Detail

  • Alfa Aesar

  • (B21609)  2-(Trifluoromethoxy)benzenesulfonamide, 99%   

  • 37526-59-3

  • 5g

  • 2624.0CNY

  • Detail

37526-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(TRIFLUOROMETHOXY)BENZENESULFONAMIDE

1.2 Other means of identification

Product number -
Other names o-Trifluormethoxybenzolsulfamid

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:37526-59-3 SDS

37526-59-3Relevant articles and documents

Design and synthesis of triazolopyrimidine acylsulfonamides as novel anti-mycobacterial leads acting through inhibition of acetohydroxyacid synthase

Patil, Vikas,Kale, Manoj,Raichurkar, Anandkumar,Bhaskar, Brahatheeswaran,Prahlad, Dwarakanath,Balganesh, Meenakshi,Nandan, Santosh,Shahul Hameed

supporting information, p. 2222 - 2225 (2014/05/06)

Novel triazolopyrimidine acylsulfonamides class of antimycobacterial agents, which are mycobacterial acetohydroxyacid synthase (AHAS) inhibitors were designed by hybridization of known AHAS inhibitors such as sulfonyl urea and triazolopyrimidine sulfonamides. This Letter describes the synthesis and SAR studies of this class of molecules by variation of two parts of the molecule, the phenyl and triazolopyrimidine rings. SAR study describes optimisation of enzyme potency, whole cell potency and evidence of mechanism of action.

Method of preparing 2-trifluoromethoxy-benzenesulphonamide

-

, (2008/06/13)

2-Trifluoromethoxy-benzenesulphonamide, of the formula (I), STR1 which can be used as intermediate for the preparation of certain herbicidally active compounds is obtained in very high yield and high purity by a process in which halogenated trifluorometho

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