1423439-33-1

Basic information

• Product Name: (E)-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-en-1-yl)benzaldehyde
• Synonyms: (E)-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-en-1-yl)benzaldehyde
• CAS NO: 1423439-33-1
• Molecular Weight: 450.199
• Mol File: 1423439-33-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-en-1-yl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-en-1-yl)benzaldehyde(1423439-33-1)
• EPA Substance Registry System: (E)-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-en-1-yl)benzaldehyde(1423439-33-1)

Safety Data

• Hazardous Substances Data: 1423439-33-1(Hazardous Substances Data)

Upstream product

• 355-43-1 n-perfluorohexyl iodide 
• 19955-99-8 3-ethenylbenzaldehyde 
• 335-56-8 1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane 

Relevant articles and documents

A general synthesis of fluoroalkylated alkenes by palladium-catalyzed Heck-type reaction of fluoroalkyl bromides

An efficient palladium-catalyzed Heck-type reaction of fluoroalkyl halides, including perfluoroalkyl bromides, trifluoromethyl iodides, and difluoroalkyl bromides, has been developed. The reaction proceeds under mild reaction conditions with high efficiency and broad substrate scope, and provides a general and straightforward access to fluoroalkylated alkenes which are of interest in life and material sciences.