862201-37-4

Basic information

• Product Name: Morpholine, 4-[[4-(5-phenyl-1H-pyrrol-3-yl)phenyl]methyl]-
• CAS NO: 862201-37-4
• Molecular Formula: C21H22N2O
• Molecular Weight: 318.418
• Mol File: 862201-37-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Morpholine, 4-[[4-(5-phenyl-1H-pyrrol-3-yl)phenyl]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Morpholine, 4-[[4-(5-phenyl-1H-pyrrol-3-yl)phenyl]methyl]-(862201-37-4)
• EPA Substance Registry System: Morpholine, 4-[[4-(5-phenyl-1H-pyrrol-3-yl)phenyl]methyl]-(862201-37-4)

Safety Data

• Hazardous Substances Data: 862201-37-4(Hazardous Substances Data)

Upstream product

• 82413-63-6 4-(morpholin-4-ylmethyl)benzaldehyde 
• 862201-28-3 3-(4-morpholin-4-ylmethyl-phenyl)-4-nitro-1-phenyl-butan-1-one 
• 51359-78-5 4-(bromomethyl)benzaldehyde 

Relevant articles and documents

A modular synthesis of unsymmetrical tetraarylazadipyrromethenes

A stepwise route to unsymmetrical tetraarylazadipyrromethenes by a condensation of 2,4-diaryl-5-nitroso-pyrroles with 2,4-diarylpyrroles is described. This modular building-block approach allows for the introduction of up to four different aryl substituents on the azadipyrromethene and is tolerant of a varied substituent set. An efficient synthesis of the 2,4-diarylpyrroles building blocks from 1,3-diaryl-4-nitro-butan-1-ones by nitro hydrolysis to a keto-aldehyde and subsequent ammonia condensation reaction has been achieved. The facile conversion of 2,4-diarylpyrroles into their α-nitroso analogues by their reaction with sodium nitrite generated the second building block required for the synthesis.