296776-75-5

Basic information

• Product Name: 3-(3-methylphenyl)-1,2-benzisothiazole 1,1-dioxide
• Synonyms: 3-(3-methylphenyl)-1,2-benzisothiazole 1,1-dioxide
• CAS NO: 296776-75-5
• Molecular Weight: 257.313
• Mol File: 296776-75-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-(3-methylphenyl)-1,2-benzisothiazole 1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-methylphenyl)-1,2-benzisothiazole 1,1-dioxide(296776-75-5)
• EPA Substance Registry System: 3-(3-methylphenyl)-1,2-benzisothiazole 1,1-dioxide(296776-75-5)

Safety Data

• Hazardous Substances Data: 296776-75-5(Hazardous Substances Data)

Upstream product

• 28987-79-3 m-tolylmagnesium bromide 
• 81-07-2 saccharin 
• 121905-60-0 3-methylphenylmagnesium chloride 

Downstream Products

• 296776-78-8 (S)-3-(m-tolyl)-2,3-dihydrobenzo[d]isothiazole-1,1-dioxide 
• 1356266-15-3 (E)-ethyl 2-(4,4-dioxido-8b-(m-tolyl)-1H-azeto[1,2-b]benzo[d]isothiazol-2(8bH)-ylidene)acetate 
• 1356266-36-8 ethyl 9b-(m-tolyl)-1,9b-dihydrobenzo[d]pyrrolo[1,2-b]isothiazole-3-carboxylate 5,5-dioxide 
• 1356266-27-7 ethyl 9b-(m-tolyl)-3,9b-dihydrobenzo[d]pyrrolo[1,2-b]isothiazole-1-carboxylate 5,5-dioxide 
• 1418635-35-4 C₂₁H₁₉NO₃S 
• 1418635-31-0 C₂₀H₁₇NO₂S 
• 1609405-67-5 (E)-methyl 3-(2-(1,1-dioxidobenzo[d]isothiazol-3-yl)-4-methylphenyl)acrylate 

Relevant articles and documents

Efficient visible-light photocatalytic aerobic oxidation of cyclic sulfamides to imines

A highly efficient photocatalytic aerobic oxidation of cyclic sulfamides to synthesize cyclic N-sulfonyl imines with Ir(ppy)2(dtbpy)PF6 as photocatalyst is reported. These environmentally friendly transformations exihibit good to excellent isolated yields and good generality with respect to both five-membered and six-membered cyclic sulfamides.

Iridium(III)-Catalyzed Selective and Mild C-H Amidation of Cyclic N-Sulfonyl Ketimines with Organic Azides

A general protocol for iridium catalyzed direct C?H amidation of cyclic N-sulfonyl ketimines using sulfonyl, acyl and aryl azides as nitrogen source is reported herein. The reaction takes place at room temperature with acyl and aryl azides, while an elevated temperature needed with sulfonyl azides to furnish aminated sultams in excellent yields with complete chemo and regioselectivity, thus providing a robust and environmentally benign process to the synthesis of aminosultams. (Figure presented.).

Sultams: catalyst systems for asymmetric reduction of a C=N intermediate biological compositions and methods for making the sultams

Biologically active sultams are disclosed which have potent anti-HIV activity. Solution methods of syntheses, which use a new catalyst for the asymmetric reduction of a C═N intermediate, are described. Biological compositions and method of treating mammal