93704-58-6

Basic information

• Product Name: Acetamide, N-[2-[(5-chloro-1H-indol-3-yl)amino]phenyl]-
• CAS NO: 93704-58-6
• Molecular Formula: C16H14ClN3O
• Molecular Weight: 299.76
• Mol File: 93704-58-6.mol

Chemical Properties

• CAS DataBase Reference: Acetamide, N-[2-[(5-chloro-1H-indol-3-yl)amino]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-[2-[(5-chloro-1H-indol-3-yl)amino]phenyl]-(93704-58-6)
• EPA Substance Registry System: Acetamide, N-[2-[(5-chloro-1H-indol-3-yl)amino]phenyl]-(93704-58-6)

Safety Data

• Hazardous Substances Data: 93704-58-6(Hazardous Substances Data)

Upstream product

• 72561-51-4 5-chloro-1H-indol-3-ylamine 
• 213542-01-9 5-chloro-3-nitro-1H-indole 
• 17422-32-1 5-chloro-1H-indole 
• 108-24-7 acetic anhydride 
• 93704-54-2 N-(5-Chloro-1H-indol-3-yl)-benzene-1,2-diamine 

Relevant articles and documents

Synthesis of Substituted Indolobenzodiazepine Derivatives

Various substituted-7,12-dihydroindolobenzodiazepines (4a-e) have been prepared from the corresponding 3-aminoindoles (1a-e) through Ullmann reaction with o-chloroaniline, acylation of the resulting 3-(o-aminophenylamino)indoles (2a-e) and cyclization of amides (3a-e) with POCl3.Similar systems have also been synthesized from ethyl 3-bromoindole-2-carboxylates (6a-e).The bromo esters react with o-phenylenediamine to give ethyl 3-(o-aminophenylamino)indole-2-carboxylates (7a-e) which undergo cyclization in the presence of PPA to yield 5,6,7,12-tetrahydroindolobenzodiazepin-6-ones (8a-e).