741681-54-9

Basic information

• Product Name: 1H-Pyrrole-1-carboxamide,N,N-dimethyl-(9CI)
• Synonyms: 1H-Pyrrole-1-carboxamide,N,N-dimethyl-(9CI)
• CAS NO: 741681-54-9
• Molecular Formula: C7H10N2O
• Molecular Weight: 138.169
• Product Categories: AMIDE;AMINETERTIARY
• Mol File: 741681-54-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrole-1-carboxamide,N,N-dimethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-1-carboxamide,N,N-dimethyl-(9CI)(741681-54-9)
• EPA Substance Registry System: 1H-Pyrrole-1-carboxamide,N,N-dimethyl-(9CI)(741681-54-9)

Safety Data

• Hazardous Substances Data: 741681-54-9(Hazardous Substances Data)

Usage

Classification

Carboxamide

Derivative of

Pyrrole (a five-membered aromatic heterocycle)

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Physical form

White to off-white solid

Solubility

Soluble in organic solvents such as ethanol and acetone

Handling precautions

Potential health and environmental hazards

Upstream product

• 109-97-7 pyrrole 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 

Relevant articles and documents

Site- and Regioselective Monoalkenylation of Pyrroles with Alkynes via Cp?CoIII Catalysis

A site-, regio-, syn-, and monoselective alkenylation of dimethylcarbamoyl-protected pyrroles proceeded using a catalytic amount of [Cp?Co(CH3CN)3](SbF6)2 and KOAc. A variety of internal alkynes with several fun

Regioselective C2 oxidative olefination of indoles and pyrroles through cationic rhodium(III)-Catalyzed C-H bond activation

Be economic with your atoms! An efficient Rh-catalyzed oxidative olefination of indoles and pyrroles with broad substrate scope and tolerance is reported (see scheme). The catalytic reaction proceeds with excellent regio- and stereoselectivity. The directing group N,N-dimethylcarbamoyl was crucial for the reaction and could be removed easily. Copyright