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2905-23-9

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2905-23-9 Usage

Chemical Properties

clear yellow to orange-red liquid

Uses

2-Chlorobenzenesulfonyl chloride is used as an organic chemical synthesis intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 2905-23-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2905-23:
(6*2)+(5*9)+(4*0)+(3*5)+(2*2)+(1*3)=79
79 % 10 = 9
So 2905-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl2O2S/c7-5-3-1-2-4-6(5)11(8,9)10/h1-4H

2905-23-9 Well-known Company Product Price

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

  • (A14054)  2-Chlorobenzenesulfonyl chloride, 98%   

  • 2905-23-9

  • 5g

  • 713.0CNY

  • Detail
  • Alfa Aesar

  • (A14054)  2-Chlorobenzenesulfonyl chloride, 98%   

  • 2905-23-9

  • 25g

  • 2992.0CNY

  • Detail
  • Alfa Aesar

  • (A14054)  2-Chlorobenzenesulfonyl chloride, 98%   

  • 2905-23-9

  • 100g

  • 11246.0CNY

  • Detail
  • Aldrich

  • (546925)  2-Chlorobenzenesulfonylchloride  97%

  • 2905-23-9

  • 546925-5G

  • 1,092.78CNY

  • Detail
  • Aldrich

  • (546925)  2-Chlorobenzenesulfonylchloride  97%

  • 2905-23-9

  • 546925-25G

  • 4,229.55CNY

  • Detail

2905-23-9SDS

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-Chlorobenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names Benzenesulfonyl chloride,2-chloro

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:2905-23-9 SDS

2905-23-9Relevant articles and documents

Facile synthesis of sulfonyl chlorides/bromides from sulfonyl hydrazides

Chen, Rongxiang,Xu, Shaohong,Shen, Fumin,Xu, Canran,Wang, Kaikai,Wang, Zhanyong,Liu, Lantao

, (2021/09/20)

A simple and rapid method for efficient synthesis of sulfonyl chlorides/bromides from sulfonyl hydrazide with NXS (X = Cl or Br) and late-stage conversion to several other functional groups was described. A variety of nucleophiles could be engaged in this transformation, thus permitting the synthesis of complex sulfonamides and sulfonates. In most cases, these reactions are highly selective, simple, and clean, affording products at excellent yields.

Aromatic Chlorosulfonylation by Photoredox Catalysis

Májek, Michal,Neumeier, Michael,Jacobi von Wangelin, Axel

, p. 151 - 155 (2017/01/17)

Visible-light photoredox catalysis enables the efficient synthesis of arenesulfonyl chlorides from anilines. The new protocol involves the convenient in situ preparation of arenediazonium salts (from anilines) and the reactive gases SO2and HCl (from aqueous SOCl2). The photocatalytic chlorosulfonylation operates at mild conditions (room temperature, acetonitrile/water) with low catalyst loading. Various functional groups are tolerated (e.g., halides, azides, nitro groups, CF3, SF5, esters, heteroarenes). Theoretical and experimental studies support a photoredox-catalysis mechanism.

Synthesis of aryl sulfonamides via palladium-catalyzed chlorosulfonylation of arylboronic acids

Debergh, J. Robb,Niljianskul, Nootaree,Buchwald, Stephen L.

supporting information, p. 10638 - 10641 (2013/08/23)

A palladium-catalyzed method for the preparation of sulfonamides is described. The process exhibits significant functional group tolerance and allows for the preparation of a number of arylsulfonyl chlorides and sulfonamides under mild conditions.

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