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58457-24-2

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58457-24-2 Usage

Chemical Properties

Light yellow to brown powder

Check Digit Verification of cas no

The CAS Registry Mumber 58457-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,5 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58457-24:
(7*5)+(6*8)+(5*4)+(4*5)+(3*7)+(2*2)+(1*4)=152
152 % 10 = 2
So 58457-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C4HCl2NO4S2/c5-4-2(7(8)9)1-3(12-4)13(6,10)11/h1H

58457-24-2 Well-known Company Product Price

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  • Alfa Aesar

  • (A11779)  5-Chloro-4-nitrothiophene-2-sulfonyl chloride, 98%   

  • 58457-24-2

  • 1g

  • 226.0CNY

  • Detail
  • Alfa Aesar

  • (A11779)  5-Chloro-4-nitrothiophene-2-sulfonyl chloride, 98%   

  • 58457-24-2

  • 5g

  • 939.0CNY

  • Detail

58457-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-CHLORO-4-NITROTHIOPHENE-2-SULFONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 5-chloro-4-nitro-thiophene-2-sulfonyl 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:58457-24-2 SDS

58457-24-2Relevant articles and documents

-

Astrakhantseva,N.I. et al.

, (1975)

-

3-Substituted thieno[2,3-b][1,4]thiazine-6-sulfonamides. A novel class of topically active carbonic anhydrase inhibitors

Hunt,Mallorga,Michelson,Schwam,Sondey,Smith,Sugrue,Shepard

, p. 240 - 247 (2007/10/02)

3-Aminoalkyl derivatives of thieno[2,3-b][1,4]thiazine-6-sulfonamide were prepared for evaluation as topically active ocular hypotensive agents. The compounds described were found to be excellent in vitro inhibitors of carbonic anhydrase II and in vivo to

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