1320232-56-1

Basic information

• Product Name: methyl 1-benzyl-2,5-dimethyl-4-phenyl-1H-pyrrole-3-carboxylate
• Synonyms: methyl 1-benzyl-2,5-dimethyl-4-phenyl-1H-pyrrole-3-carboxylate
• CAS NO: 1320232-56-1
• Molecular Weight: 319.403
• Mol File: 1320232-56-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 1-benzyl-2,5-dimethyl-4-phenyl-1H-pyrrole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 1-benzyl-2,5-dimethyl-4-phenyl-1H-pyrrole-3-carboxylate(1320232-56-1)
• EPA Substance Registry System: methyl 1-benzyl-2,5-dimethyl-4-phenyl-1H-pyrrole-3-carboxylate(1320232-56-1)

Safety Data

• Hazardous Substances Data: 1320232-56-1(Hazardous Substances Data)

Upstream product

• 75-52-5 nitromethane 
• 100-52-7 benzaldehyde 
• 105-45-3 acetoacetic acid methyl ester 
• 100-46-9 benzylamine 
• 120935-94-6 methyl 4-bromo-2,5-dimethyl-1H-pyrrole-3-carboxylate 
• 98-80-6 phenylboronic acid 
• 69687-80-5 methyl 2,5-dimethyl-1H-pyrrole-3-carboxylate 
• 705-60-2 (2-nitroprop-1-enyl)benzene 
• 72002-24-5 methyl 3-(benzylamino)but-2-enoate 

Relevant articles and documents

Preparation, characterization and catalytic application of molybdenum Schiff-base complex immobilized on silica-coated Fe3O4 as a reusable catalyst for the synthesis of pyranopyrazole derivatives

A recoverable molybdenum Schiff-base complex immobilized on silica-coated Fe3O4 nanoparticles was prepared and characterized. This superparamagntic nanocatalyst, which is separable using an external magnet, can be used as an efficien

A facile and efficient synthesis of multisubstituted pyrroles from enaminoesters and nitroolefins

A facile and efficient method for the synthesis of substituted pyrroles from enaminoesters and nitroolefins is reported. This general procedure provides a wide variety of multisubstituted pyrroles in good to excellent yields under mild reaction conditions.