111865-49-7

Basic information

• Product Name: N-benzyl-1-(4-chlorophenyl)-3-butenylamine
• Synonyms: N-benzyl-1-(4-chlorophenyl)-3-butenylamine
• CAS NO: 111865-49-7
• Molecular Weight: 271.79
• Mol File: 111865-49-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-benzyl-1-(4-chlorophenyl)-3-butenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-1-(4-chlorophenyl)-3-butenylamine(111865-49-7)
• EPA Substance Registry System: N-benzyl-1-(4-chlorophenyl)-3-butenylamine(111865-49-7)

Safety Data

• Hazardous Substances Data: 111865-49-7(Hazardous Substances Data)

Upstream product

• 130517-96-3 N-[(1E)-(4-chlorophenyl)methylidene]benzenemethanamine 
• 106-95-6 allyl bromide 
• 130517-96-3 N-(4-chlorobenzylidene)benzylamine 
• 24850-33-7 allyltributylstanane 
• 104-88-1 4-chlorobenzaldehyde 
• 100-46-9 benzylamine 

Downstream Products

• 4727-72-4 1-benzyl-4-hydroxypiperidine 

Relevant articles and documents

Allylstannane Allylation of Aldimines Activated by Chlorotrimethylsilane

Aldimines activated by chlorotrimethylsilane reacted with allylstannane to give the corresponding homoallylic amines with excellent yields.

Mg and Zn mediated allylation of imines with allyl bromide

Both aldimines and ketamines are allylated under simple Barbier-type conditions using allyl bromide and commercial magnesium foil or zinc dust in tetrahydrofuran at room temperature.

Indium mediated Barbier-type allylation of aldimines in alcoholic solvents

Barbier-type allylation of unactivated aldimines with allyl bromides in the presence of indium powder took place rapidly in alcoholic solvents to give homoallylic amines in fair to good yields.