917341-34-5

Basic information

• Product Name: (2E)-N-(3-bromophenyl)-3-phenylprop-2-enamide
• Synonyms: (2E)-N-(3-bromophenyl)-3-phenylprop-2-enamide
• CAS NO: 917341-34-5
• Molecular Weight: 302.17
• Mol File: 917341-34-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2E)-N-(3-bromophenyl)-3-phenylprop-2-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-N-(3-bromophenyl)-3-phenylprop-2-enamide(917341-34-5)
• EPA Substance Registry System: (2E)-N-(3-bromophenyl)-3-phenylprop-2-enamide(917341-34-5)

Safety Data

• Hazardous Substances Data: 917341-34-5(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 101349-79-5 2-phenylvinyl iodide 
• 591-19-5 m-Bromoaniline 
• 140-10-3 (E)-3-phenylacrylic acid 
• 102-92-1 cinnamoyl chloride 

Downstream Products

• 99455-13-7 5-bromo-2-chloroquinoline 
• 99455-15-9 7-bromo-2-chloro-quinoline 
• 99465-09-5 5-bromoquinolin-2(1H)-one 
• 99465-10-8 7-bromo-1,2-dihydroquinolin-2-one 

Relevant articles and documents

Electron-Catalyzed Aminocarbonylation: Synthesis of α,β-Unsaturated Amides from Alkenyl Iodides, CO, and Amines

Aminocarbonylation of alkenyl iodides with CO and amines proceeded under heating to produce α,β-unsaturated amides in good yields (23 examples, 71% average yield). This catalyst-free method exhibited good functional-group tolerance, and open a straightforward access to functionalized acrylamides, as illustrated by the synthesis of Ilepcimide. A hybrid radical/ionic mechanism involving chain electron transfer is proposed for this transformation.

2-QUINOLINONE AND 2-QUINOXALINONE- DERIVATIVES AND THEIR USE AS ANTIBACTERIAL AGENTS

The present invention relates to compounds of Formula (I) : and pharmaceutically acceptable salts thereof, to their use in the treatment of bacterial infections, and to their methods of preparation.