41208-22-4

Basic information

• Product Name: 2-PIPERIDIN-1-YL-1-PHENYLETHYLAMINE
• Synonyms: 2-PIPERIDIN-1-YL-1-PHENYLETHYLAMINE;1-Phenyl-2-piperidin-1-yl-ethylamine;1-(2-Amino-2-phenylethyl)piperidine
• CAS NO: 41208-22-4
• Molecular Formula: C₁₃H₂₀N₂
• Molecular Weight: 204.31
• Mol File: 41208-22-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-PIPERIDIN-1-YL-1-PHENYLETHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PIPERIDIN-1-YL-1-PHENYLETHYLAMINE(41208-22-4)
• EPA Substance Registry System: 2-PIPERIDIN-1-YL-1-PHENYLETHYLAMINE(41208-22-4)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 41208-22-4(Hazardous Substances Data)

Upstream product

• 10591-92-1 (E)-1-phenyl-2-(piperidin-1-yl)ethan-1-one oxime 
• 64-17-5 ethanol 
• 41208-54-2 2-phenyl-2,3,5,6,7,8-hexahydro-imidazo[1,2-a]pyridine 
• 4641-62-7 1-phenyl-2-piperidino-ethanone; hydrochloride 
• 7101-04-4 (E/Z)-1-(2-hydroximino-2-phenylethyl)piperidine 

Downstream Products

• 41208-66-6 2-phenyl-perhydroimidazo[1,2-a]pyridine 
• 41208-54-2 2-phenyl-2,3,5,6,7,8-hexahydro-imidazo[1,2-a]pyridine 
• 41208-34-8 1-(2-Acetylamino-2-phenyl-ethyl)piperidin 

Relevant articles and documents

Dehydrogenation of cyclic tertiary amines with neighbouring of enantiomeric nucleophiles

For stereochemical investigation of their dehydrogenation, the enantiomers of the aminoalcohols 1, 2, and 3 were prepared from optically active sources, while the enantiomers of the diamines 8 and 9 were available by resolution of the racemates. The pure antipodes of 1, 2, and 3 reacted with mercury(II)-EDTA by a twofold dehydrogenation via intermediate participation of the neighbouring alcoholic group to the optically active lactams 5, 6, and 7 under complete retention of configuration. In the same manner the diamines 8 and 9 generated by four electron withdrawal the cycloamidines 10 and 11.