40872-77-3

Basic information

• Product Name: 3,5-Diphenyl-2-forMylpyrrole
• Synonyms: 3,5-Diphenyl-2-forMylpyrrole;3,5-diphenyl-1H-Pyrrole-2-carboxaldehyde;3,5-diphenyl-1H-pyrrole-2-carbaldehyde
• CAS NO: 40872-77-3
• Molecular Formula: C₁₇H₁₃NO
• Molecular Weight: 247.29122
• Mol File: 40872-77-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 473.2±45.0 °C(Predicted)
• Appearance: /
• Density: 1.177±0.06 g/cm3(Predicted)
• PKA: 14.90±0.50(Predicted)
• CAS DataBase Reference: 3,5-Diphenyl-2-forMylpyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Diphenyl-2-forMylpyrrole(40872-77-3)
• EPA Substance Registry System: 3,5-Diphenyl-2-forMylpyrrole(40872-77-3)

Safety Data

• Hazardous Substances Data: 40872-77-3(Hazardous Substances Data)

Upstream product

• 15814-32-1 1,5-diphenylpenta-1,4-diyn-3-ol 
• 94-41-7 benzalacetophenone 
• 131475-18-8 3,5-diphenyl-1H-pyrrole-2-carbonitrile 
• 3274-56-4 2,4-diphenylpyrrole 
• 68-12-2 N,N-dimethyl-formamide 
• 6268-00-4 4-oxo-2,4-diphenylbutanenitrile 
• 40047-93-6 (3,5-diphenyl-1H-pyrrol-2-yl)(3,5-diphenylpyrrol-2-ylidene)amine 
• 6277-67-4 4-nitro-1,3-diphenyl-butan-1-one 
• 87774-48-9 3,5-diphenyl-3,4-dihydro-2H-pyrrole 
• 93-61-8 N-methyl-N-phenylformamide 

Downstream Products

• 858271-82-6 (3,5-diphenyl-pyrrol-2-yl)-methanol 
• 154793-50-7 1,3,5,7-tetraphenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 
• 13401-33-7 2-[(3,5-diphenyl-2H-pyrrol-2-ylidene)methyl]-3,5-diphenyl-1H-pyrrole 

Relevant articles and documents

Effects of π-extension on pyrrole hemithioindigo photoswitches

The most red-shifted hemithioindigo photoswitches have been identified through systematic introduction of aryl units to a parent pyrrole hemithioindigo photoswitch. Increasing the size of the 5′-aryl substituent is ineffective at producing further redshif

Modular De novo Synthesis of Unsymmetrical BODIPY Dyes Possessing Four Different Aryl Substituents

A modular synthesis of unsymmetrical BODIPY dyes based on a [6π] electrocyclization to construct both pyrrole rings is presented. The products carry four aryl moieties in positions 1, 3, 5, and 7, which can be freely selected, as well as optional substitution in positions 2 and 8. The method employs acetophenones, benzaldehydes as well as glycine nitrile or glycine ethyl ester as the key building blocks.

A new synthesis of symmetric boraindacene (BODIPY) dyes

BODIPY dyes were synthesized from pyrrole-2-carbaldehyde derivatives in high yields; this constitutes a new approach to this dye framework. The Royal Society of Chemistry.