849796-05-0

Basic information

• Product Name: 2-Propenal, 3-(pentafluorophenyl)-, (2E)-
• CAS NO: 849796-05-0
• Molecular Formula: C9H3F5O
• Molecular Weight: 222.114
• Mol File: 849796-05-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propenal, 3-(pentafluorophenyl)-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenal, 3-(pentafluorophenyl)-, (2E)-(849796-05-0)
• EPA Substance Registry System: 2-Propenal, 3-(pentafluorophenyl)-, (2E)-(849796-05-0)

Safety Data

• Hazardous Substances Data: 849796-05-0(Hazardous Substances Data)

Upstream product

• 653-37-2 perfluorobenzaldehyde 
• 2136-75-6 (triphenylphosphoranylidene)acetaldehyde 
• 1736-60-3 1-allyl-2,3,4,5,6-pentafluorobenzene 

Downstream Products

• 1013421-30-1 3-(perfluorophenyl)-2-phenylisoxazolidin-5-one 
• 56693-03-9 1,2,3,4,5-pentafluoro-6-[(1E,3E)-4-phenyl-1,3-butadien-1-yl]benzene 
• 849796-16-3 (1E,3S)-1-pentafluorophenylhexa-1,5-dien-3-ol 
• 849796-25-4 2,2,2-trichloro-N-[(1S,2E)-1-pentafluorophenylhexa-2,5-dienyl]acetamide 

Relevant articles and documents

Regioselective α-Deuteration of Michael Acceptors Mediated by Isopropylamine in D2O/AcOD

Site-specific hydrogen/deuterium exchange is an important method to access deuterated compounds for chemical and biological studies. Herein is reported the first method for the regioselective α-deuteration of enals and enones. The transformation features D2O and AcOD as deuterium sources and amines as organocatalysts. The deuteration strategy is scalable and works on enals with a variety of substituted arene or heterocycle motifs as well as enones. The method has been applied to the synthesis of deuterated drug precursors.

CARBOLINE ANTIPARASITICS

The present invention provides Formula (1 ) compounds that are gamma-carbolines, Formula (1) wherein R1 a, R1 b, R1 c, R1d, R2, R3, and "— " are as defined herein; veterinary acceptable salts thereof, and stereoisomers thereof, which act as parasiticides,

Regiospecific photoisomerization of fluorinated (E,E)-1,4-diphenyl-1,3- butadienes

Photoisomerization of five fluorinated E,E-1-(R-phenyl)-4-phenyl-1,3- butadienes in solution (R = 1: p-monofluoro, 2: m,m′-difluoro, 3: m,m′,p-trifluoro, 4: o,o′,m,m′-tetrafluoro, 5: o,o′,m,m′,p-pentafluoro) was investigated via direct irradiation. Our results indicated that cis-trans photoisomerization of the fluorinated 1,4-diphenyl-1,3-butadienes in the excited singlet state took place exclusively at the CC bonds closer to the fluorine substituents.