94673-95-7

Basic information

• Product Name: 2-[3-(4-methoxy-phenyl)-3-oxo-propyl]-1,1-dioxo-1,2-dihydro-1λ⁶-benzo[d]isothiazol-3-one
• Synonyms: 2-[3-(4-methoxy-phenyl)-3-oxo-propyl]-1,1-dioxo-1,2-dihydro-1λ⁶-benzo[d]isothiazol-3-one
• CAS NO: 94673-95-7
• Molecular Weight: 345.376
• Mol File: 94673-95-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-[3-(4-methoxy-phenyl)-3-oxo-propyl]-1,1-dioxo-1,2-dihydro-1λ⁶-benzo[d]isothiazol-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[3-(4-methoxy-phenyl)-3-oxo-propyl]-1,1-dioxo-1,2-dihydro-1λ⁶-benzo[d]isothiazol-3-one(94673-95-7)
• EPA Substance Registry System: 2-[3-(4-methoxy-phenyl)-3-oxo-propyl]-1,1-dioxo-1,2-dihydro-1λ⁶-benzo[d]isothiazol-3-one(94673-95-7)

Safety Data

• Hazardous Substances Data: 94673-95-7(Hazardous Substances Data)

Upstream product

• 67-68-5 dimethyl sulfoxide 
• 81-07-2 saccharin 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 35999-20-3 3-chloro-4'-methoxypropiophenone 

Relevant articles and documents

Oxidative C-S bond cleavage reaction of DMSO for C-N and C-C bond formation: New Mannich-type reaction for β-amino ketones

A novel oxidative C-S bond cleavage reaction of DMSO for N-methylation and subsequent C-C bond formation is described. A series of aryl ketones as well as acetone derivatives could be selectively converted into the corresponding β-amino ketones. Mechanistic studies suggested that N-methylation between imine and DMSO was involved in the reaction.