1353749-41-3

Basic information

• Product Name: ethyl 1-butyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylate
• Synonyms: ethyl 1-butyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylate
• CAS NO: 1353749-41-3
• Molecular Weight: 285.386
• Mol File: 1353749-41-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 1-butyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-butyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylate(1353749-41-3)
• EPA Substance Registry System: ethyl 1-butyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylate(1353749-41-3)

Safety Data

• Hazardous Substances Data: 1353749-41-3(Hazardous Substances Data)

Upstream product

• 102-96-5 (2-nitroethenyl)benzene 
• 141-97-9 ethyl acetoacetate 
• 109-73-9 N-butylamine 
• 5065-81-6 ethyl 3-(butylamino)but-2-enoate 
• 5153-67-3 nitrostyrene 

Relevant articles and documents

Synthesis of polysubstituted pyrroles via a gold(I)-catalyzed tandem three-component reaction at room temperature

A gold(I)-catalyzed three-component reaction of β-nitrostyrenes with 1,3-dicarbonyl compounds and primary amines to form polysubstituted pyrroles has been developed at room temperature in ethanol. The key advantages of the three-component reaction are the

Gold-catalyzed cascade C-C and C-N bond formation: Synthesis of polysubstituted indolequinones and pyrroles

The combination of Ph3PAuCl and AgOTf was proven to be an efficient catalyst for the cascade C-C and C-N bond formation reactions from enamines and bromoquinones or nitroolefins. This protocol affords a straightforward method for the synthesis of polysubstituted indolequinones and pyrroles in good yields.