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594-44-5

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594-44-5 Usage

Chemical Properties

clear light brownish to pinkish-purple liquid

Synthesis Reference(s)

Journal of the American Chemical Society, 61, p. 2548, 1939 DOI: 10.1021/ja01878a085

Check Digit Verification of cas no

The CAS Registry Mumber 594-44-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 594-44:
(5*5)+(4*9)+(3*4)+(2*4)+(1*4)=85
85 % 10 = 5
So 594-44-5 is a valid CAS Registry Number.
InChI:InChI=1/C2H5ClO2S/c1-2-6(3,4)5/h2H2,1H3

594-44-5 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (B23723)  Ethanesulfonyl chloride, 98+%   

  • 594-44-5

  • 25g

  • 293.0CNY

  • Detail
  • Alfa Aesar

  • (B23723)  Ethanesulfonyl chloride, 98+%   

  • 594-44-5

  • 100g

  • 637.0CNY

  • Detail
  • Alfa Aesar

  • (B23723)  Ethanesulfonyl chloride, 98+%   

  • 594-44-5

  • 500g

  • 2275.0CNY

  • Detail
  • Aldrich

  • (471542)  Ethanesulfonylchloride  ≥99%

  • 594-44-5

  • 471542-100ML

  • 710.19CNY

  • Detail
  • Aldrich

  • (471542)  Ethanesulfonylchloride  ≥99%

  • 594-44-5

  • 471542-500ML

  • 2,279.16CNY

  • Detail

594-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethanesulfonyl chloride

1.2 Other means of identification

Product number -
Other names chloroethylsulfone

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:594-44-5 SDS

594-44-5Relevant articles and documents

Copper-Catalyzed N-Directed Distal C(sp3)-H Sulfonylation and Thiolation with Sulfinate Salts

Chen, Guang-Le,He, Shi-Hui,Cheng, Liang,Liu, Feng

supporting information, p. 8338 - 8342 (2021/10/25)

We herein report a selective and catalytic C(sp3)-H functionalization approach to access amines bearing organo-sulfonyl and organo-thiol groups. This reaction proceeds through a cascade process of N-radical formation, alkyl radical formation via 1,5-HAT, and C-S bond formation, thereby offering a series of functionalized amines. This method could enable primary, secondary, and tertiary C(sp3)-H sulfonylation and thiolation and also exhibits good functional group tolerance.

One-pot synthesis of sulfonamides and sulfonyl azides from thiols using chloramine-T

Maleki, Behrooz,Hemmati, Saba,Tayebee, Reza,Salemi, Sirous,Farokhzad, Yasaman,Baghayeri, Mehdi,Zonoz, Farrokhzad Mohammadi,Akbarzadeh, Elahe,Moradi, Rohollah,Entezari, Azam,Abdi, Mohammad Reza,Ashrafi, Samaneh Sedigh,Taimazi, Fereshteh,Hashemi, Majid

, p. 2147 - 2151 (2013/12/04)

A convenient synthesis of sulfonamides and sulfonyl azides from thiols is described. In situ preparation of sulfonyl chlorides from thiols was accomplished by oxidation with chloramine-T (=N-chlorotosylamide=N-chloro-4- methylbenzenesulfonamide), tetrabutylammonium chloride (Bu4NCl), and H2O. The sulfonyl chlorides were then further allowed to react with excess amine or NaN3 in the same pot.

Simple synthesis of sulfonyl chlorides from thiol precursors and derivatives by NaClO2-mediated oxidative chlorosulfonation

Yang, Zhanhui,Zheng, Yongpeng,Xu, Jiaxi

supporting information, p. 2165 - 2169 (2013/10/22)

A simple method to synthesize diverse sulfonyl chlorides through NaClO 2-mediated oxidative chlorosulfonation of S-alkyl isothiourea salts is presented. The approach features safe operation, environmental friendliness, convenient purification procedures, and delivers high yields of up to 96%. The procedure is also applicable to substrates such as thiols, disulfides, thioacetates, and xanthates. It is a versatile and convenient method for the synthesis of various sulfonyl chlorides from different thiol precursors and derivatives. Georg Thieme Verlag Stuttgart, New York.

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