1352310-62-3

Basic information

• Product Name: ((2R,3R,4R,5R)-5-(2-(benzyloxy)ethyl)-1-cyclopropyl-2,4-dimethylpiperidin-3-yl)methanol
• Synonyms: ((2R,3R,4R,5R)-5-(2-(benzyloxy)ethyl)-1-cyclopropyl-2,4-dimethylpiperidin-3-yl)methanol
• CAS NO: 1352310-62-3
• Molecular Weight: 317.472
• Mol File: 1352310-62-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((2R,3R,4R,5R)-5-(2-(benzyloxy)ethyl)-1-cyclopropyl-2,4-dimethylpiperidin-3-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: ((2R,3R,4R,5R)-5-(2-(benzyloxy)ethyl)-1-cyclopropyl-2,4-dimethylpiperidin-3-yl)methanol(1352310-62-3)
• EPA Substance Registry System: ((2R,3R,4R,5R)-5-(2-(benzyloxy)ethyl)-1-cyclopropyl-2,4-dimethylpiperidin-3-yl)methanol(1352310-62-3)

Safety Data

• Hazardous Substances Data: 1352310-62-3(Hazardous Substances Data)

Upstream product

• 15301-37-8 3-ethoxycarbonyl-3-penten-2-one 
• 5470-84-8 4-benzyloxybutanal 
• 1352310-45-2 C₂₂H₃₃NO₃ 
• 1352310-16-7 C₁₉H₂₆O₅ 

Relevant articles and documents

Organocatalytically enantioselective approach to polysubstituted tetrahydropyridines and piperidines

A convenient and highly enantioselective method for assembly of functionalized 1,2,3,4,5-pentasubstituted tetrahydropyridines and piperidines was developed. This method relies on preparing the required enantiopure cyclic semi-acetals via an organocatalyzed Michael addition/cyclization cascade reaction of aldehydes and α-keto-α,β-unsaturated esters, and subsequent reductive amination/condensation with primary amines. Copyright