223432-76-6

Basic information

• Product Name: N-benzyl-1H-pyrrole-1-carboxamide
• Synonyms: N-benzyl-1H-pyrrole-1-carboxamide
• CAS NO: 223432-76-6
• Molecular Weight: 200.24
• Mol File: 223432-76-6.mol

Chemical Properties

• CAS DataBase Reference: N-benzyl-1H-pyrrole-1-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-1H-pyrrole-1-carboxamide(223432-76-6)
• EPA Substance Registry System: N-benzyl-1H-pyrrole-1-carboxamide(223432-76-6)

Safety Data

• Hazardous Substances Data: 223432-76-6(Hazardous Substances Data)

Upstream product

• 109-97-7 pyrrole 
• 3173-56-6 benzyl isothiocyanate 
• 56880-01-4 1-phenoxycarbonyl pyrrole 
• 100-46-9 benzylamine 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 223432-88-0 2-Benzyl-pyrrolo[1,2-c]pyrimidine-1,3,4-trione 
• 223432-91-5 2-Benzyl-4-hydroxy-3,4-dihydro-2H-pyrrolo[1,2-c]pyrimidin-1-one 
• 223432-86-8 2-Benzyl-2,3-dihydro-pyrrolo[1,2-c]pyrimidine-1,4-dione 

Relevant articles and documents

Highly stereoselective ruthenium(II)-catalyzed direct C2- syn -alkenylation of indoles with alkynes

A carboamide-directed ruthenium-catalyzed C2-hydroindolation of alkynes has been described. This transformation provides a rapid access to free (N-H) C2-syn-alkenylated indole derivatives with the assistance of copper(II) salts, in which the directing group is removed via a one-pot process.

A simple direct phosgeneless route to N-heteroaryl unsymmetrical ureas

A new simple approach to the synthesis of unsymmetrical ureas HetNC(O)NRR′ (HetNH = pyrrole, indole, carbazole; R, R′ = H, alkyl, aryl) has been explored, which involves the direct reaction of the N-phenoxycarbonyl derivatives of pyrrole, indole and carba

Synthesis of 1,2-dihydropyrrolo[1,2-c]pyrimidin-l-ones

1,2-Dihydropyrrolo[1,2-c]pyrimidin-1-ones 2 have been synthesised from pyrrole. We have developed a versatile procedure for the introduction of substituents into the pyrrolopyrimidinones 2, at positions 5 or 7 as desired, and as required by our plans for