634878-89-0

Basic information

• Product Name: 2-allyl-1-benzylpiperidine
• Synonyms: 2-allyl-1-benzylpiperidine
• CAS NO: 634878-89-0
• Molecular Weight: 215.338
• Mol File: 634878-89-0.mol

Chemical Properties

• CAS DataBase Reference: 2-allyl-1-benzylpiperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-allyl-1-benzylpiperidine(634878-89-0)
• EPA Substance Registry System: 2-allyl-1-benzylpiperidine(634878-89-0)

Safety Data

• Hazardous Substances Data: 634878-89-0(Hazardous Substances Data)

Upstream product

• 120153-68-6 N-benzylpiperidine-2-carbonitrile 
• 106-95-6 allyl bromide 
• 20056-98-8 N-benzyl-N-methoxyamine 
• 29872-25-1 N-benzylpiperidine N-oxide 
• 89656-44-0 2‐allylpiperidine 
• 100-39-0 benzyl bromide 

Relevant articles and documents

Synthesis of (±)-Lasubine II Using N-Methoxyamines

The synthesis of (±)-lasubine II has been achieved through a three-component allylation capitalizing on the unique properties of N-methoxyamines. This reaction enabled the installation of all the carbon atoms of lasubineII in a single operation. The N-met

Stereocontrol in N-directed hydroboration: Synthesis of amino alcohols related to the piperidine alkaloids

Treatment of 2-(2'-alkenyl)-piperidine boranes with iodine or triflic acid induces internal hydroboration with high regiocontrol, even with a terminal alkene (R H). Good stereocontrol is possible for the N-benzyl substrates. Comparisons with acyclic model

A New and Practical Procedure for the Bruylants Reaction. Zinc-Mediated Synthesis of Tertiary Homoallylamines and β-Aminoesters

N,N-Disubstituted α-aminonitriles undergo Bruylants reaction under Barbier and Reformatsky conditions with activated halides, in the presence of zinc and 10 mol% HOAc. The high yields and the simple operational conditions make this reaction an appealing, approach to N,N-disubstituted homoallylamines and β-aminoesters.