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001284

001284-1g



Methanesulfinic acid, sodium salt


CAS Number: 20277-69-4
   
Molecular Formula: CH3NaO2S
   
Molecular Weight: 102.09
   
MDL Number: MFCD00040392


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001284-1g
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001284-5g
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001284-25g
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001284-100g
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001284-1Kg
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Purity:90%
Mp:222-226°(dec.)
 
Pictograms:
Signal Word:Warning
Hazard Statements:H302, H315, H319, H335
Precautionary Statements:P261, P301 + P330 + P331, P302 + P352, P304 + P340, P305 + P351 + P338
SDS: See MSDS
 

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A reagent that can react with electrophilic carbon atoms to form methyl sulfones in a single step.1 Applied in stereoselective synthesis of (E)-alkenyl sulfones from alkenes or alkynes,2 preparation of branched allylic sulfones by iridium-catalyzed allylation,3 reaction with α-halo ketones under microwave irradiation to  afford the corresponding β-keto sulfones,4 introduction of a sulfone group to pyridines and diazines,5 synthesis of β-hydroxy-sulfones via opening of epoxides in ionic liquid,6 preparation of aryl and alkenylsulfones from the cross-coupling reaction with organoboronic acids,7 and synthesis of vinyl sulfones.8 Starting material for synthesis of aryl sulfoxides and sulfonium salts in trifluoromethanesulfonic acid as a novel sulfurizing agent.9 Catalyst used in preparation of heteroarenecarbonitriles,10 and in synthesis of 2-aroylquinoxalines, 1-aroylphthalazines, and 4-aroylcinnolines.11

Reference

1.        J. Am. Chem. Soc. 195375, 5582.
2.        Synlett 2011, 1308.
3.        Org. Lett. 201012, 92.
4.        Green Chem. Lett. Rev. 20081, 179.
5.        Tetrahedron Lett. 200950, 1928.
6.        J. Sulfur Chem. 200728, 513.
7.        Tetrahedron 200763, 7667.
8.        Synthesis 2007, 1465.
9.        Chem. Comm. 1996, 2099.
10.        Heterocycles 199849, 405.
11.        Heterocycles 199439, 345.

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