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ChemicalBook--->CAS DataBase List--->6953-60-2

6953-60-2

6953-60-2 Structure

6953-60-2 Structure
IdentificationMore
[Name]

S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE
[CAS]

6953-60-2
[Synonyms]

2-(ACETYLTHIO)SUCCINIC ANHYDRIDE
LABOTEST-BB LT00159681
S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE
Ethanethioicacid,S-(tetrahydro-2,5-dioxo-3-furanyl)ester
(acetylthio)succinic anhydride
(S)-Acetyl-2-mercaptosuccinicanhydride
2-(Acetylthio)succinic anhydride, SAMSA
3-(Acetylthio)tetrahydrofuran-2,5-dione
[EINECS(EC#)]

230-135-2
[Molecular Formula]

C6H6O4S
[MDL Number]

MFCD00005526
[Molecular Weight]

174.17
[MOL File]

6953-60-2.mol
Chemical PropertiesBack Directory
[Melting point ]

83-86 °C (lit.)
[Boiling point ]

354.3±31.0 °C(Predicted)
[density ]

1.42±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[Sensitive ]

Hygroscopic
[CAS DataBase Reference]

6953-60-2(CAS DataBase Reference)
[EPA Substance Registry System]

Ethanethioic acid, S-(tetrahydro-2,5-dioxo-3-furanyl) ester (6953-60-2)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE(6953-60-2)MS
S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE(6953-60-2)1HNMR
S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE(6953-60-2)13CNMR
S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE(6953-60-2)IR1
S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE(6953-60-2)IR2
S-ACETYLMERCAPTOSUCCINIC ANHYDRIDE(6953-60-2)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

S-Acetylmercaptosuccinic anhydride, 90%(6953-60-2)
[Sigma Aldrich]

6953-60-2(sigmaaldrich)
Hazard InformationBack Directory
[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.
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