162104-35-0

Basic information

• Product Name: C₁₁H₁₃N₃O₇S
• CAS NO: 162104-35-0
• Molecular Weight: 331.306
• Mol File: 162104-35-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₁₁H₁₃N₃O₇S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₁H₁₃N₃O₇S(162104-35-0)
• EPA Substance Registry System: C₁₁H₁₃N₃O₇S(162104-35-0)

Safety Data

• Hazardous Substances Data: 162104-35-0(Hazardous Substances Data)

Upstream product

• 162104-37-2 N-Acetyl-N-(2,6-dioxo-piperidin-1-yl)-3-nitro-benzenesulfonamide 
• 162104-36-1 N-(2,6-Dioxo-piperidin-1-yl)-3-nitro-benzenesulfonamide 
• 108-55-4 glutaric anhydride, 
• 6655-77-2 3-nitrophenylsulfonohydrazide 

Downstream Products

• 162104-36-1 N-(2,6-Dioxo-piperidin-1-yl)-3-nitro-benzenesulfonamide 
• 162104-37-2 N-Acetyl-N-(2,6-dioxo-piperidin-1-yl)-3-nitro-benzenesulfonamide 

Relevant articles and documents

Alkaline Hydrolysis and Alcoholysis of N-(Arylsulfonylamino)- and N-(N-Acetylarylsulfonylamino)succin- and -glutarimides

Alkaline hydrolysis and alcoholysis of N-(arylsulfonylamino)- and N-(N-acetylarylsulfonylamino)-succin- and glutarimides have been studied. The reaction outcome is determined both by the size of the imide ring and by the substituent on the imide nitrogen atom. Alkaline hydrolysis of N-(N-acetylarylsulfonylamino)-succin- and -glutarimides is characterized by different order of elimination of the acetyl group and opening of the imide ring. Heating of N-(arylsulfonylamino)glutarimides in methanol in the presence of sodium methoxide results in formation of methyl 5-(arylsulfonylhydrazino)-5-oxopentanoates, whereas the reaction with N-(arylsulfonylamino)succinimides stops at the stage of formation of the corresponding sodium salt.