198694-02-9

Basic information

• Product Name: (E)-2-Phenyl-ethenesulfonic acid (2,2-dimethoxy-ethyl)-methyl-amide
• Synonyms: (E)-2-Phenyl-ethenesulfonic acid (2,2-dimethoxy-ethyl)-methyl-amide
• CAS NO: 198694-02-9
• Molecular Weight: 285.364
• Mol File: 198694-02-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-2-Phenyl-ethenesulfonic acid (2,2-dimethoxy-ethyl)-methyl-amide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-Phenyl-ethenesulfonic acid (2,2-dimethoxy-ethyl)-methyl-amide(198694-02-9)
• EPA Substance Registry System: (E)-2-Phenyl-ethenesulfonic acid (2,2-dimethoxy-ethyl)-methyl-amide(198694-02-9)

Safety Data

• Hazardous Substances Data: 198694-02-9(Hazardous Substances Data)

Upstream product

• 52147-97-4 trans 2-phenylethenesulfonyl chloride 
• 122-07-6 N-(methyl)aminoacetaldehyde dimethyl acetal 

Downstream Products

• 198694-08-5 (E)-2-Phenyl-ethenesulfonic acid methyl-[2-(phenyl-hydrazono)-ethyl]-amide 
• 198694-03-0 (E)-2-Phenyl-ethenesulfonic acid methyl-(2-oxo-ethyl)-amide 

Relevant articles and documents

Stereoselective synthesis of isoxazole and pyrazole annulated sultams via intramolecular 1,3-dipolar cycloaddition reactions

Functionalized isothiazoloisoxazole-4,4-dioxide, pyrazoloisothiazole-1,1-dioxide, [1,2]thiazinoisoxazole-4,4-dioxide and benzo[1,2]thiazinoisoxazole-4,4-dioxide systems have been obtained by intramolecular 1,3-dipolar cycloaddition, starting from substituted α- and β-sulfonamides.