846-22-0

Basic information

• Product Name: 1-phenyl-2,5-di(thiophen-2-yl)-1H-pyrrole
• Synonyms: 1-phenyl-2,5-di(thiophen-2-yl)-1H-pyrrole
• CAS NO: 846-22-0
• Molecular Weight: 307.44
• Mol File: 846-22-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-phenyl-2,5-di(thiophen-2-yl)-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-2,5-di(thiophen-2-yl)-1H-pyrrole(846-22-0)
• EPA Substance Registry System: 1-phenyl-2,5-di(thiophen-2-yl)-1H-pyrrole(846-22-0)

Safety Data

• Hazardous Substances Data: 846-22-0(Hazardous Substances Data)

Upstream product

• 4298-52-6 2-ethynyl-thiophene 
• 62-53-3 aniline 
• 13196-35-5 3-(dimethylamino)-1-(thiophen-2-yl)propan-1-one 
• 98-03-3 thiophene-2-carbaldehyde 
• 13669-05-1 1,4-bis(thiophen-2-yl)butane-1,4-dione 
• 100-46-9 benzylamine 

Relevant articles and documents

Copper(II)-Promoted, One-Pot Conversion of 1-Alkynes with Anhydrides or Primary Amines to the Respective 2,5-Disubstituted Furans or Pyrroles under Microwave Irradiation Conditions

Furans and pyrroles are prepared from 1-alkynes by using a Cu(II)-promoted, one-pot, microwave irradiation method. Glaser coupling of 1-alkynes and cyclization of the resulting 1,3-diyne in the presence of an anhydride or a primary amine results in the formation of the respective 2,5-diaryl- or 2,5-dialkyl-substituted furans and pyrroles.

Strong π-delocalization and substitution effect on electronic properties of dithienylpyrrole-containing bipyridine ligands and corresponding ruthenium complexes

The first dithienylpyrrole (DTP)-based bipyridine ligands has been prepared and coordinated with ruthenium to give the corresponding homoleptic complexes. Bipyridine was bound at pyrrole (DTP1) or thiophene (DTP2) ring. A strong bath

N-substituted pyrrole synthesis by Paal-Knorr condensation using recyclable cationic exchange resin in water

(Chemical Equation Presented) Cationic exchange resin has been utilized for the first time as a novel and recyclable heterogeneous catalyst for the synthesis of N-substituted pyrroles from variety of 1,4-diketones and aniline. This simple synthesis has been accomplished with excellent yields. The recovered catalyst can be reused for subsequent runs with only a gradual decrease in activity.