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6953-60-2

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  • S-Acetylmercaptosuccinicanhydride,2-(Acetylthio)succinicanhydride,Mercaptosuccinicacidanhydride

    Cas No: 6953-60-2

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6953-60-2 Usage

General Description

S-Acetylmercaptosuccinic anhydride is an amine reactive reagent, containing a sulfhydryl group. The anhydride region opens up, when attacked by an amine nucleophile, forming amine linkage. However, during this ring opening reaction, a free carboxylate group is formed rendering the molecule negatively charged. Activity to proteins and conformation of the molecule us affected by the charge reversal.

Check Digit Verification of cas no

The CAS Registry Mumber 6953-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6953-60:
(6*6)+(5*9)+(4*5)+(3*3)+(2*6)+(1*0)=122
122 % 10 = 2
So 6953-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O4S/c1-3(7)11-4-2-5(8)10-6(4)9/h4H,2H2,1H3/t4-/m0/s1

6953-60-2 Well-known Company Product Price

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  • Aldrich

  • (197327)  S-Acetylmercaptosuccinicanhydride  96%

  • 6953-60-2

  • 197327-5G

  • 1,003.86CNY

  • Detail
  • Aldrich

  • (197327)  S-Acetylmercaptosuccinicanhydride  96%

  • 6953-60-2

  • 197327-25G

  • 3,465.54CNY

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6953-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(2,5-dioxooxolan-3-yl) ethanethioate

1.2 Other means of identification

Product number -
Other names S-Acetylmercaptosuccinic acid anhydride

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

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More Details:6953-60-2 SDS

6953-60-2Downstream Products

6953-60-2Relevant articles and documents

Regioselective ring opening of thiomalic acid anhydrides by carbon nucleophiles. Synthesis and X-ray structure elucidation of novel thiophenone derivatives

Kikionis, Stefanos,McKee, Vickie,Markopoulos, John,Igglessi-Markopoulou, Olga

experimental part, p. 3711 - 3716 (2009/09/05)

Novel and promising thiophenone derivatives were synthesised by regioselective ring opening of activated thiomalic acid anhydrides, with a variety of active methylene nucleophiles via a C-acylation/cyclisation process involving an S-C bond formation. This

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