1421605-75-5

Basic information

• Product Name: 4-phenyl-2H-pyrrolo[3,4-c]quinoline
• Synonyms: 4-phenyl-2H-pyrrolo[3,4-c]quinoline
• CAS NO: 1421605-75-5
• Molecular Weight: 244.296
• Mol File: 1421605-75-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-phenyl-2H-pyrrolo[3,4-c]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-2H-pyrrolo[3,4-c]quinoline(1421605-75-5)
• EPA Substance Registry System: 4-phenyl-2H-pyrrolo[3,4-c]quinoline(1421605-75-5)

Safety Data

• Hazardous Substances Data: 1421605-75-5(Hazardous Substances Data)

Upstream product

• 7473-93-0 (E)-3-(2-nitrophenyl)-1-phenylprop-2-en-1-one 
• 16714-25-3 2-azidobenzaldehyde 
• 552-89-6 2-nitro-benzaldehyde 
• 108714-18-7 3-(2-aminophenyl)-1-phenyl-2-(E)-propen-1-one 
• 31541-36-3 3-benzoylmethylidene-2-oxindole 
• 1421605-62-0 methyl [2-(4-benzoyl-1H-pyrrol-3-yl)phenyl]carbamate 

Relevant articles and documents

Synthesis of 2H-pyrrolo[3,4-C]quinoline via an Aldol/Van Leusen/Staudinger/aza-Wittig sequence

An aldol/van Leusen/Staudinger/aza-Wittig reaction for the preparation of the derivatives of 2H-pyrrolo[3,4-c]quinolines from 2-azidobenzaldehyde, acetyl compounds, and tosylmethyl isocyanide was developed. The process involves an aldol condensation of 2-

3-Phenacylideneoxindoles with tosylmethyl isocyanide and MeOH through C-C bond cleavage: Facile synthesis of pyrrole and 2H-pyrrolo[3,4-c]quinoline derivatives

A novel reaction of 3-phenacylideneoxindoles (1) with tosylmethyl isocyanide (2a) and MeOH through C-C bond cleavage has been developed. The reaction proceeded under mild conditions, providing a powerful synthetic tool for the construction of pyrrole derivatives (3) from easily accessible starting materials and synthesis of 2H-pyrrolo[3,4-c]quinolines (4) by further dehydration of 3.