791626-56-7

Basic information

• Product Name: 2-Propenamide, N-(4-fluorophenyl)-3-phenyl-, (2E)-
• CAS NO: 791626-56-7
• Molecular Formula: C15H12FNO
• Molecular Weight: 241.265
• Mol File: 791626-56-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propenamide, N-(4-fluorophenyl)-3-phenyl-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenamide, N-(4-fluorophenyl)-3-phenyl-, (2E)-(791626-56-7)
• EPA Substance Registry System: 2-Propenamide, N-(4-fluorophenyl)-3-phenyl-, (2E)-(791626-56-7)

Safety Data

• Hazardous Substances Data: 791626-56-7(Hazardous Substances Data)

Upstream product

• 140-10-3 (E)-3-phenylacrylic acid 
• 371-40-4 4-fluoroaniline 
• 102-92-1 Cinnamoyl chloride 

Downstream Products

• 22614-75-1 6-fluoro-1H-quinolin-2-one 
• 791626-57-8 6-fluoroquinolin-2-amine 
• 77119-53-0 2-chloro-6-fluoro-quinoline 

Relevant articles and documents

Substituted Hantzsch Esters as Versatile Radical Reservoirs in Photoredox Reactions

Substituted Hantzsch esters can act as radical reservoirs in photoredox reactions, steadily releasing a carbon radical and a hydrogen atom radical in the absence of an additional electron acceptor. We propose that radical release by substituted Hantzsch esters occurs via a mechanism involving an internal redox cycle. Cinnamidecinnamides, styrenes, α,β-unsaturated acids, and diarylethenes could be alkylated smoothly with these reagents. (Figure presented.).

NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS

Unsaturated nitrogen heterocyclic compounds of formula (I): (I), as defined in the specification, compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, Huntington's Disease, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.