141054-41-3

Basic information

• Product Name: 1H-Pyrrole-2-acetic acid, 5-benzoyl-, ethyl ester
• CAS NO: 141054-41-3
• Molecular Formula: C15H15NO3
• Molecular Weight: 257.289
• Mol File: 141054-41-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-2-acetic acid, 5-benzoyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2-acetic acid, 5-benzoyl-, ethyl ester(141054-41-3)
• EPA Substance Registry System: 1H-Pyrrole-2-acetic acid, 5-benzoyl-, ethyl ester(141054-41-3)

Safety Data

• Hazardous Substances Data: 141054-41-3(Hazardous Substances Data)

Upstream product

• 4778-25-0 (1H-pyrrol-2-yl)acetic acid ethyl ester 
• 98-88-4 benzoyl chloride 
• 611-74-5 N,N-dimethylbenzamide 
• 7697-46-3 phenyl(1H-pyrrol-2-yl)methanone 
• 3278-34-0 ethyl 2-(ethoxythiocarbonylthio)acetate 

Downstream Products

• 153602-69-8 2-benzoyl-4-phenylpyrano<4,3-b>pyrrol-6(1H)-one 
• 153602-62-1 3,5-dibenzoylpyrrol-2-ylacetic acid 
• 153602-70-1 isobutyl 2-benzoyl-6-oxo-4-phenylpyrano<4,3-b>pyrrole-1-carboxylate 
• 141054-45-7 5-benzoyl-pyrrole-2-acetic acid 
• 141054-44-6 ethyl 3,5-dibenzoylpyrrol-2-ylacetate 

Relevant articles and documents

Et3B-Mediated radical alkylation of pyrroles and indoles

An efficient Et3B-mediated oxidative radical substitution of substituted pyrroles and indoles using xanthate based radical chemistry in the presence of iron(II) sulfate is described. Unsubstituted indole gave only low yield or failed in the process. 2-Cyanofuran and 2-benzoylthiophene did not afford the corresponding alkylated products under these conditions.

Pyrrole-2,3-quinodimethane Analogues in the Synthesis of Indoles. Part 2. Synthesis and Diels-Alder Reactions of 1,6-Dihydropyranopyrrol-6(1H)-ones

The pyranopyrrol-6-ones 7-9, 12 and 13 are stable cyclic analogues of pyrrole-2,3-quinodimethane, and undergo Diels-Alder reaction with a range of alkynes to give, after loss of carbon dioxide, indoles.