1425668-87-6

Basic information

• Product Name: benzyl (2R,6R)-4,4-dimethoxy-2-methyl-6-nonylpiperidine-1-carboxylate
• CAS NO: 1425668-87-6
• Molecular Weight: 419.605
• Mol File: 1425668-87-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl (2R,6R)-4,4-dimethoxy-2-methyl-6-nonylpiperidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (2R,6R)-4,4-dimethoxy-2-methyl-6-nonylpiperidine-1-carboxylate(1425668-87-6)
• EPA Substance Registry System: benzyl (2R,6R)-4,4-dimethoxy-2-methyl-6-nonylpiperidine-1-carboxylate(1425668-87-6)

Safety Data

• Hazardous Substances Data: 1425668-87-6(Hazardous Substances Data)

Upstream product

• 1425666-89-2 (R)-benzyl [5-(diethoxyphosphoryl)-4-oxopentan-2-yl]carbamate 
• 142035-70-9 methyl (R)-3-(benzyloxycarbonylamino)-butanoate 
• 1425667-34-0 (R,E)-benzyl [4-oxo-pentadec-5-en-2-yl]carbamate 
• 149-73-5 trimethyl orthoformate 

Relevant articles and documents

Access to 2,6-disubstituted piperidines: Control of the diastereoselectivity, scope, and limitations. applications to the stereoselective synthesis of (-)-solenopsine A and alkaloid (+)-241D

Scope and limitations in the diastereoselective preparation of 2,6-cis or 2,6-trans disubstituted piperidines are described, through intramolecular reaction of chiral β′-carbamate-α,β-unsaturated ketone. This methodology has been applied to the total synthesis of a few well chosen examples, such as (-)-solenopsine A and alkaloid (+)-241D.