101289-19-4

Basic information

• Product Name: ethyl 2,4-dimethyl-5-(phenylcarbamoyl)-1H-pyrrole-3-carboxylate
• Synonyms: ethyl 2,4-dimethyl-5-(phenylcarbamoyl)-1H-pyrrole-3-carboxylate
• CAS NO: 101289-19-4
• Molecular Weight: 286.331
• Mol File: 101289-19-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 2,4-dimethyl-5-(phenylcarbamoyl)-1H-pyrrole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2,4-dimethyl-5-(phenylcarbamoyl)-1H-pyrrole-3-carboxylate(101289-19-4)
• EPA Substance Registry System: ethyl 2,4-dimethyl-5-(phenylcarbamoyl)-1H-pyrrole-3-carboxylate(101289-19-4)

Safety Data

• Hazardous Substances Data: 101289-19-4(Hazardous Substances Data)

Upstream product

• 2199-51-1 2,4-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 141-97-9 ethyl acetoacetate 
• 84321-36-8 3-phenylcarbamoyl-4-methyl-1,2,5-selenadiazole 
• 5442-91-1 3,5-dimethyl-1H-pyrrole-2,4-dicarboxylic acid 4-ethyl ester 
• 62-53-3 aniline 
• 2352-40-1 2-(hydroxyimino)-3-oxo-N-phenylbutanamide 

Downstream Products

• 625-82-1 2,4-dimethyl-1H-pyrrole 

Relevant articles and documents

Pyrrole studies. Part 44. Synthesis of potentially biologically active pyrroloylanilines

The direct reaction of acid labile pyrrolecarboxylic acids with anilines in the presence of N,N'-dicyclohexylcarbodiimide provides an efficient general synthesis of pyrroloylanilines.

A Novel One-pot Synthesis of Pyrroles from 1,2,5-Selenadiazole and 1,3-Diketones

A one-pot reaction of 4-methyl-3-phenylcarbamoyl-1,2,5-selenadiazole 2 and 1,3-diketones in the presence of zinc dust and acetic acid gave 1,2-disubstituted 3-methyl-4-phenylcarbamoylpyrroles 3.