1581259-53-1

Basic information

• Product Name: ethyl 2-[N,N-bis(3,5-dimethylphenyl)sulfamoyl]acetate
• Synonyms: ethyl 2-[N,N-bis(3,5-dimethylphenyl)sulfamoyl]acetate
• CAS NO: 1581259-53-1
• Molecular Weight: 375.489
• Mol File: 1581259-53-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 2-[N,N-bis(3,5-dimethylphenyl)sulfamoyl]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-[N,N-bis(3,5-dimethylphenyl)sulfamoyl]acetate(1581259-53-1)
• EPA Substance Registry System: ethyl 2-[N,N-bis(3,5-dimethylphenyl)sulfamoyl]acetate(1581259-53-1)

Safety Data

• Hazardous Substances Data: 1581259-53-1(Hazardous Substances Data)

Upstream product

• 108-69-0 3,5-dimethylaminoaniline 
• 172975-69-8 3,5-dimethylphenyl boronic acid 
• 55896-93-0 ethyl 2-(chlorosulfonyl)acetate 
• 5369-25-5 bis-(3,5-dimethylphenyl)-amine 

Downstream Products

• 1581259-07-5 ethyl 2-[N,N-bis(3,5-dimethylphenyl)sulfamoyl]-2-diazoacetate 
• 1581258-84-5 ethyl 4,6-dimethyl-1-(3,5-dimethylphenyl)-1,3-dihydrobenzo[c]isothiazole-3-carboxylate 2,2-dioxide 

Relevant articles and documents

Synthesis of benzo-γ-sultams via the Rh-catalyzed aromatic C-H functionalization of diazosulfonamides

An efficient synthesis of 1-aryl-benzo-γ-sultams, 1-aryl-1,3-dihydrobenzo[c]isothiazole-2,2-dioxides, was achieved in 65-99% yields via the Rh-catalyzed intramolecular aromatic C-H functionalization of N,N-diaryl diazosulfonamides with 0.5 mol% Rh2(oct)4 as the catalyst. This journal is the Partner Organisations 2014.