26977-44-6

Basic information

• Product Name: N³-(4-chlorophenyl)-1H-indole-3-carboxamide
• Synonyms: N³-(4-chlorophenyl)-1H-indole-3-carboxamide
• CAS NO: 26977-44-6
• Molecular Weight: 270.718
• Mol File: 26977-44-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N³-(4-chlorophenyl)-1H-indole-3-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N³-(4-chlorophenyl)-1H-indole-3-carboxamide(26977-44-6)
• EPA Substance Registry System: N³-(4-chlorophenyl)-1H-indole-3-carboxamide(26977-44-6)

Safety Data

• Hazardous Substances Data: 26977-44-6(Hazardous Substances Data)

Upstream product

• 59496-25-2 Indole-3-carbonyl chloride 
• 106-47-8 4-chloro-aniline 
• 1613-88-3 4-chloro-N-hydroxybenzamide 
• 120-72-9 indole 
• 132401-91-3 3-(4-chlorophenyl)-1,4,2-dioxazol-5-one 
• 942-24-5 3-methoxycarbonylindole 
• 771-50-6 1H-indole-3-carboxylic acid 
• 5457-28-3 3-cyano-1H-indole 
• 1204518-00-2 (4-chlorophenyl)(mesityl)iodonium trifluoromethanesulfonate 

Downstream Products

• 752222-42-7 N³-(4-chlorophenyl)-1H-indole-3-carbothioamide 

Relevant articles and documents

1,4,2-Dioxazol-5-ones as Isocyanate Equivalents: Chemoselective Non-Metal-Catalyzed Carboxamidation of Indoles

1,4,2-Dioxazol-5-ones are known to undergo decarboxylation under thermal conditions followed by Lossen s rearrangement to give isocyanates. Described herein is the in situ trapping of the isocyanates by indoles to give indole-3-carboxamides in good to exc

Synthesis of 4,6-disubstituted-2-(1H-indol-3-yl)-benzothiazoles

A new four-step synthesis of substituted 2-(1H-indol-3-yl)benzothiazoles is described, using N3-phenyl-1H-indole-3-carbothioamides as key intermediates. The structure of the obtained products was determined by IR, 1H, 13C NMR and MS spectral methods.