84760-10-1

Usage

Chemical Class

Sulfonamides

Molecular Weight

133.16 g/mol

Usage

Solvent, Surfactant, Reagent in Organic Synthesis

Versatility

Valuable and Versatile Compound in Chemistry and Related Industries.

Downstream Products

• 99922-44-8 4,8-Diacetyl-3,7-bis(2-chlorphenyl)-1,5,2,6-dithiadiazocan-1,1,5,5-tetraoxid 
• 99922-47-1 4,8-Diacetyl-3,7-bis(2,6-dichlorphenyl)-1,5,2,6-dithiadiazocan-1,1,5,5-tetraoxid 
• 99922-45-9 4,8-Diacetyl-3,7-bis(2-fluorphenyl)-1,5,2,6-dithiadiazocan-1,1,5,5-tetraoxid 
• 99922-46-0 4,8-Diacetyl-3,7-bis(2-bromphenyl)-1,5,2,6-dithiadiazocan-1,1,5,5-tetraoxid 
• 96355-46-3 5-Acetyl-3,4-diphenyl-1,2-thiazol-1,1-dioxid 
• 99922-48-2 4,8-Diacetyl-3,7-bis(3-phenoxyphenyl)-1,5,2,6-dithiadiazocan-1,1,5,5-tetraoxid 
• 96355-49-6 N-(2-Oxopropylsulfonyl)-benzamid 
• 96355-67-8 5-Acetyl-2,6-diphenyl-1,4,3-oxathiazinan-4,4-dioxid 
• 96355-68-9 6-Acetyl-3,5-diphenyl-1,2,4-thiadiazinan-1,1-dioxid 
• 96355-70-3 3-Phenyl-1,2-thiazinan-5-on-1,1-dioxid 
• 96355-69-0 (E)-2-Oxo-4-phenyl-3-butensulfonamid 
• 96355-42-9 2-Hydroxy-4-oxo-2-phenyl-5-sulfamoylpentansaeure-ethylester 

Relevant academic research and scientific papers

2-ketosulfonamides and process for their preparation

The invention relates to new 2-ketosulfonamides of the formula STR1 and to a process for their preparation, wherein the 3-amino-2-sulfamoylalk-2-enoic acid esters of the formula STR2 obtained by reacting 3-aminoalk-2-enoic acid esters of the formula STR3 with amidosulfonyl chlorides of the formula X-SO2 -NH-R2, are subjected to hydrolysis and decarboxylation. The invention also relates to the 3-amino-2-sulfamoylalk-2-enoic acid esters which can be isolated as intermediates.

2-Ketosulfonamides

The invention relates to new 2-ketosulfonamides of the general formula STR1 and to a process for their preparation, which process comprises oxidizing compounds of the general formula with manganese dioxide in a readily volatile, oxidation-stable organic solvent, preferably acetone or acetonitrile.