92173-66-5

Basic information

• Product Name: 2-Propenenitrile,3-(1H-benzimidazol-1-yl)-,(Z)-(9CI)
• Synonyms: 2-Propenenitrile,3-(1H-benzimidazol-1-yl)-,(Z)-(9CI)
• CAS NO: 92173-66-5
• Molecular Formula: C10H7N3
• Molecular Weight: 0
• Product Categories: BENZIMIDAZOLE
• Mol File: 92173-66-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propenenitrile,3-(1H-benzimidazol-1-yl)-,(Z)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenenitrile,3-(1H-benzimidazol-1-yl)-,(Z)-(9CI)(92173-66-5)
• EPA Substance Registry System: 2-Propenenitrile,3-(1H-benzimidazol-1-yl)-,(Z)-(9CI)(92173-66-5)

Safety Data

• Hazardous Substances Data: 92173-66-5(Hazardous Substances Data)

Upstream product

• 51-17-2 benzoimidazole 
• 32837-87-9 3-hydroxy-3-methyl-1-cyano-1-butyne 
• 32837-88-0 4-hydroxy-4-methylhex-2-ynenitrile 
• 107-13-1 acrylonitrile 

Relevant articles and documents

Copper-Catalyzed Inter/Intramolecular N-Alkenylation of Benzimidazoles via Tandem Processes Involving Selectively Mild Iodination of sp3 C-H Bond at α-Position of Ester

Inter/intramolecular approaches to sp2 C-N bond formation of N-alkenyl benzimidazoles have been accomplished in the presence of an iodide anion associated with a copper catalyst. Both intermolecular and intramolecular reactions included tandem processes, in which selective iodination of sp3 C-H bond at the α-position of ester under mild conditions was demonstrated for the first time. Tandem reactions involving sp3 C-H activation via α-iodo ester intermediate under copper catalysis efficiently provided more than 20 novel azole compounds, and free radicals were not involved in this transformation.