208177-33-7

Basic information

• Product Name: (4-CHLORO-PHENYL)-(2,7-DICHLORO-10-METHYL-10H-INDOLO[3,2-B]QUINOLIN-11-YL)-METHYL-AMINE
• Synonyms: (4-CHLORO-PHENYL)-(2,7-DICHLORO-10-METHYL-10H-INDOLO[3,2-B]QUINOLIN-11-YL)-METHYL-AMINE
• CAS NO: 208177-33-7
• Molecular Formula: C23H16Cl3N3
• Molecular Weight: 440.75
• Mol File: 208177-33-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-CHLORO-PHENYL)-(2,7-DICHLORO-10-METHYL-10H-INDOLO[3,2-B]QUINOLIN-11-YL)-METHYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (4-CHLORO-PHENYL)-(2,7-DICHLORO-10-METHYL-10H-INDOLO[3,2-B]QUINOLIN-11-YL)-METHYL-AMINE(208177-33-7)
• EPA Substance Registry System: (4-CHLORO-PHENYL)-(2,7-DICHLORO-10-METHYL-10H-INDOLO[3,2-B]QUINOLIN-11-YL)-METHYL-AMINE(208177-33-7)

Safety Data

• Hazardous Substances Data: 208177-33-7(Hazardous Substances Data)

Upstream product

• 26772-93-0 N-(4-chlorophenyl)-N-methylformamide 

Relevant articles and documents

Umpoled Vilsmeier reagents. The chemistry of aminochlorocarbenes derived from Vilsmeier reagents by the action of bases

Vilsmeier reagents such as N-methyl-N-phenylchloroiminium chloride are readily deprotonated by tert-amines even in POCl3 solution. The resulting transient intermediates, aminochlorocarbenes, are nucleophilic (i.e. umpoled Vilsmeier reagents) and are trapped with electrophiles. In this way dimers [1,2-bis(N-methylanilino)-1,2-dichloroethanes] 3, 'trimers' (indolo[3,2-b]quinolininium chlorides) 4 and 5, 'tetramers' (2,2′-bis-indoles) 11 and isatins 9 and 10 are accessible in one-pot processes from the formanilide.