1152652-64-6

Basic information

• Product Name: (E)-1-[3-(4-chlorophenyl)allyl]-1,2,3,4-tetrahydroquinoline
• Synonyms: (E)-1-[3-(4-chlorophenyl)allyl]-1,2,3,4-tetrahydroquinoline
• CAS NO: 1152652-64-6
• Molecular Weight: 283.801
• Mol File: 1152652-64-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-1-[3-(4-chlorophenyl)allyl]-1,2,3,4-tetrahydroquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-[3-(4-chlorophenyl)allyl]-1,2,3,4-tetrahydroquinoline(1152652-64-6)
• EPA Substance Registry System: (E)-1-[3-(4-chlorophenyl)allyl]-1,2,3,4-tetrahydroquinoline(1152652-64-6)

Safety Data

• Hazardous Substances Data: 1152652-64-6(Hazardous Substances Data)

Upstream product

• 635-46-1 1,2,3,4-tetrahydroisoquinoline 
• 170938-14-4 (E)-3-(4-chlorophenyl)allyl acetate 
• 105643-16-1 (1'R,S)-1-(4-chlorophenyl)-2-propene-1-acetate 
• 1092381-52-6 C₁₁H₁₁ClO₂ 

Relevant articles and documents

Palladium nanoparticle-catalyzed C-N bond formation. A highly regio- and stereoselective allylic amination by allyl acetates

(Chemical Equation Presented) Palladium nanoparticles, generated in situ from the reaction of palladium(II) chloride, have been demonstrated to be an efficient catalyst for C-N bond formation. A variety of aliphatic and aromatic amines have been allylated by substituted and unsubstituted allyl acetates in high yields by using palladium nanoparticles in the presence of a base without any ligand. The allylations are highly regio- and stereoselective.