1172142-67-4

Basic information

• Product Name: methyl 2-[N-allyl-N-(4-chlorophenyl)sulfamoyl]acetate
• Synonyms: methyl 2-[N-allyl-N-(4-chlorophenyl)sulfamoyl]acetate
• CAS NO: 1172142-67-4
• Molecular Weight: 303.766
• Mol File: 1172142-67-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-[N-allyl-N-(4-chlorophenyl)sulfamoyl]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-[N-allyl-N-(4-chlorophenyl)sulfamoyl]acetate(1172142-67-4)
• EPA Substance Registry System: methyl 2-[N-allyl-N-(4-chlorophenyl)sulfamoyl]acetate(1172142-67-4)

Safety Data

• Hazardous Substances Data: 1172142-67-4(Hazardous Substances Data)

Upstream product

• 56146-83-9 chlorosulfonyl-acetic acid methyl ester 
• 13519-80-7 N-allyl-4-chloroaniline 

Downstream Products

• 1172142-78-7 C₁₂H₁₄Br₂ClNO₄S 

Relevant articles and documents

Facile access to bicyclic sultams with methyl 1-sulfonylcyclopropane-l- carboxylate moieties

N-(2,3-Dibromopropyl)- and N-(3,4-dibromobutyl)(methoxycarbonyl) methanesulfanilides upon treatment with potassium carbonate in DMF furnish, methyl 3-aryl-2,2-dioxo-2thia-3-azabicyclo[n.1.0]alkane-1.-carboxylates in yields ranging from 54 to 84% (10 examples). The starting materials were obtained by sulfonylation of N-alkenylanilines with methyl (chlorosulfonyl) acetate and. subsequent bromination. For the N-alkenylanil.in.es (10 examples, 60-77% yield) an efficient new synthesis employing a 2-nitrophenylsulfonyl substituent as a protective as well as an activating group has been developed. The 4-methoxyphenyl (PMP) group could easily be removed, from, the sultam. nitrogen atom by treatment with cerium(IV) ammonium nitrate.