3274-54-2

Basic information

• Product Name: 2-methyl-4-phenyl-1H-pyrrole
• Synonyms: 2-methyl-4-phenyl-1H-pyrrole
• CAS NO: 3274-54-2
• Molecular Weight: 157.215
• Mol File: 3274-54-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-methyl-4-phenyl-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-4-phenyl-1H-pyrrole(3274-54-2)
• EPA Substance Registry System: 2-methyl-4-phenyl-1H-pyrrole(3274-54-2)

Safety Data

• Hazardous Substances Data: 3274-54-2(Hazardous Substances Data)

Upstream product

• 6947-14-4 2-methyl-4-phenyl-pyrrolidine 
• 3274-63-3 2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 161560-98-1 1,5-dimethyl-3-phenyl-1H-pyrrole-2,4-dicarboxylic acid diethyl ester 
• 67-64-1 acetone 
• 7654-06-0 3-phenyl-2H-azirine 
• 16717-64-9 1-azidostyrene 
• 100-42-5 styrene 
• 102921-26-6 (1,2-dibromoethyl)benzene 
• 613-89-8 2-Aminoacetophenone 
• 884866-01-7 1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole 
• 1006062-36-7 1-(4-methylbenzenesulfonyl)-2-methyl-4-phenyl-1H-pyrrole 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 3651-13-6 5-methyl-3-phenyl-1H-pyrrole-2,4-dicarboxylic acid diethyl ester 
• 60317-41-1 ethyl 2-(hydroxyimino)-3-oxo-3-phenylpropanoate 

Downstream Products

• 13673-03-5 2-methyl-4-phenyl-1-pyrroline 
• 1192718-94-7 ethyl 2-methyl-4-phenylpyrrole-1-carboxylate 

Relevant articles and documents

A HYDROFORMYLATION ROUTE TO Β-SUBSTITUTED PYRROLES

Rhodium catalysed hydroformylation of readily available β-alkynylamines gives 3-substituted or 2,4-disubstituted pyrroles in good yields.

Pyrrole derivative as well as preparation method and application thereof

The invention belongs to the field of medical chemistry, and relates to a pyrrole derivativex as well as a preparation method and application thereof. A compound with a structure shown as a general formula (I), or one or a mixture of more of a tautomer, a

Simple two-step synthesis of 2,4-disubstituted pyrroles and 3,5-disubstituted pyrrole-2-carbonitriles from enones

The cyclocondensation of enones with aminoacetonitrile furnishes 3,4-dihydro-2H-pyrrole-2-carbonitriles which can be readily converted to 2,4-disubstituted pyrroles by microwave-induced dehydrocyanation. Alternatively, oxidation of the intermediates produ