4849-88-1

Basic information

• Product Name: (2S)-6β-(3-Furanyl)-3α-methyl-2β-(3-methyl-2-butenyl)piperidine
• Synonyms: (2S)-6β-(3-Furanyl)-3α-methyl-2β-(3-methyl-2-butenyl)piperidine;Anhydronupharamine
• CAS NO: 4849-88-1
• Molecular Formula: C₁₅H₂₃NO
• Molecular Weight: 233.34922
• Mol File: 4849-88-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 113-115 °C(Press: 3 Torr)
• Appearance: /
• Density: 0.933±0.06 g/cm3(Predicted)
• PKA: 9.54±0.10(Predicted)
• CAS DataBase Reference: (2S)-6β-(3-Furanyl)-3α-methyl-2β-(3-methyl-2-butenyl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-6β-(3-Furanyl)-3α-methyl-2β-(3-methyl-2-butenyl)piperidine(4849-88-1)
• EPA Substance Registry System: (2S)-6β-(3-Furanyl)-3α-methyl-2β-(3-methyl-2-butenyl)piperidine(4849-88-1)

Safety Data

• Hazardous Substances Data: 4849-88-1(Hazardous Substances Data)

Upstream product

• 17812-38-3 (-)-Nupharamin 
• 155203-54-6 (4R,5S)-5-azido-4,8-dimethyl-1-(3'-furyl)-6-nonen-1-one 
• 155203-53-5 (4R,5R)-4,8-dimethyl-1-(3'-furyl)-5-hydroxy-6-nonen-1-one 
• 155203-51-3 (3R,4R)-1-[1,3]Dithian-2-ylidene-3,7-dimethyl-oct-6-en-4-ol 
• 155203-52-4 (5R,6R)-6-(3-methyl-2-butenyl)-5-methyl-3,4,5,6-tetrahydro-2H-pyran-2-one 
• 259265-67-3 (4R,5R)-5-(3-methyl-2-butenyl)-4-methyl-2-hydroxytetrahydrofuran 
• 144781-72-6 (1R,2R,3R,5R)-3-(tert-Butyl-dimethyl-silanyloxy)-5-(1-chloro-1-methyl-ethyl)-2-methyl-cyclopentanecarboxylic acid methyl ester 
• 144781-81-7 methyl (3S,4R)-4-(tert-butyldimethylsiloxy)-3,7-dimethyl-6-octenoate 
• 140629-59-0 (4R,5R)-4-Methyl-5-(3-methyl-but-2-enyl)-dihydro-furan-2-one 

Downstream Products

• 29073-37-8 1-benzoyl-6c-furan-3-yl-3c-methyl-2r-(3-methyl-but-2-enyl)-piperidine 

Relevant articles and documents

Enantiospecific total syntheses of nuphar piperidine alkaloids, (-)- anhydronupharamine, (-)-nupharamine, (-)-nuphenine and (+)-3-epinupharamine

A concise enantiospecific synthesis of nuphar piperidine alkaloids was achieved by employing a regioselective carbon-carbon bond cleavage reaction of the cyclopentane derivative, having a γ-chloro carbonyl system, as a key reaction.