5425-53-6

Basic information

• Product Name: 5H,6H,7H-benzo[c]carbazole
• Synonyms: 5H,6H,7H-benzo[c]carbazole;6,7-Dihydro-5H-benzo[c]carbazole
• CAS NO: 5425-53-6
• Molecular Formula: C₁₆H₁₃N
• Molecular Weight: 219.28112
• Mol File: 5425-53-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 423.9°C at 760 mmHg
• Flash Point: 190.6°C
• Appearance: /
• Density: 1.228g/cm³
• Vapor Pressure: 5.31E-07mmHg at 25°C
• Refractive Index: 1.722
• CAS DataBase Reference: 5H,6H,7H-benzo[c]carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5H,6H,7H-benzo[c]carbazole(5425-53-6)
• EPA Substance Registry System: 5H,6H,7H-benzo[c]carbazole(5425-53-6)

Safety Data

• Hazardous Substances Data: 5425-53-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H13N/c1-2-6-12-11(5-1)9-10-15-16(12)13-7-3-4-8-14(13)17-15/h1-8,17H,9-10H2

Upstream product

• 64-17-5 ethanol 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 83160-35-4 3,4-dihydro-1H-naphthalen-2-one phenylhydrazone 

Downstream Products

• 205-25-4 benzo[c]carbazole 
• 1210468-70-4 C₅₂H₃₆N₂ 
• 1210469-12-7 C₂₈H₁₈ClN 
• 1210469-11-6 10-bromo-7-phenyl-7H-benzo[c]carbazole 
• 648432-24-0 7-phenyl-7H-benzo[c]carbazole 

Relevant articles and documents

Radical cyclisation reactions with indoles

Several radical cyclisation reactions involving indoles are described. Most notably, we have shown that radical additions to C3 of an indole are frequently facile. A dichotomy in the course of radical cyclisation reactions to C2 of the indole has also been exposed wherein 6-endo-trig cyclisations are propagated by the loss of a hydrogen atom from C2 while 5-exo-trig cyclisations are propagated by hydrogen atom abstraction at C3 from tributyltin hydride. Cyclisations involving the addition of indolyl radical intermediates to arenes have also been demonstrated.