74028-19-6

Basic information

• Product Name: 4-amino-N-[1-(1H-indol-3-yl)methyl]benzenesulfonamide
• CAS NO: 74028-19-6
• Molecular Weight: 301.369
• Mol File: 74028-19-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-amino-N-[1-(1H-indol-3-yl)methyl]benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-amino-N-[1-(1H-indol-3-yl)methyl]benzenesulfonamide(74028-19-6)
• EPA Substance Registry System: 4-amino-N-[1-(1H-indol-3-yl)methyl]benzenesulfonamide(74028-19-6)

Safety Data

• Hazardous Substances Data: 74028-19-6(Hazardous Substances Data)

Upstream product

• 487-89-8 Indole-3-carboxaldehyde 
• 63-74-1 sulfanilamide 
• 74028-03-8 4-amino-N-[1-(1H-indol-3-yl)methylidene]benzenesulfonamide 

Downstream Products

• 64299-06-5 5,6,11,12,17,18-hexahydrocyclononane[1,2-b:4,5-b':7,8-b'']triindole 

Relevant articles and documents

A practical and expeditious method for the preparation of the potential anticancer agent 5,6,11,12,17,18,23,24-octahydrocyclododeca[1,2-b:4,5-b′: 7,8-b″:10,11-b?]tetraindole (CTet)

A new synthetic method to obtain the potential anticancer agent 5,6,11,12,17,18,23,24-octahydrocyclododeca[1,2-b:4,5-b′:7, 8-b′′:10,11-b′′′]tetraindole (CTet), starting from 1H-indole-3-carboxaldehyde and sulfamide, is described. Although a mixture of CTet and cyclic indole trimer (CTr) is formed, higher CTet/CTr ratio (4:6) and CTet yield (15%) make our protocol more favorable than those reported in the literature. A discussion on the possible reaction mechanism is reported.