247259-33-2

Basic information

• Product Name: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester
• Synonyms: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester;methyl (1-benzylpiperidin-4-yl)acetate;2-[1-(benzyl)-4-piperidyl]acetic acid methyl ester;2-[1-(phenylmethyl)-4-piperidinyl]acetic acid methyl ester;methyl (1-benzylpiperidin-4-yl)acetate hydrochloride;methyl 2-[1-(phenylmethyl)-4-piperidyl]acetate;methyl 2-[1-(phenylmethyl)piperidin-4-yl]acetate;methyl 2-[1-(phenylmethyl)piperidin-4-yl]ethanoate
• CAS NO: 247259-33-2
• Molecular Formula: C15H21NO2
• Molecular Weight: 247.33274
• Mol File: 247259-33-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester(247259-33-2)
• EPA Substance Registry System: 4-piperidineacetic acid, 1-(phenylmethyl)-, methyl ester(247259-33-2)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 247259-33-2(Hazardous Substances Data)

Upstream product

• 3612-20-2 1-phenylmethyl-4-piperidone 
• 206558-34-1 C₁₅H₁₉NO₂ 
• 70199-68-7 methyl 4-pyridylacetate hydrochloride 
• 54401-85-3 pyridin-4-yl-acetic acid ethyl ester 
• 100-39-0 benzyl bromide 
• 81270-37-3 methyl piperidine-4-acetate hydrochloride 

Downstream Products

• 865626-97-7 (±)-3-(1-benzylpiperidin-4-yl)-4-hydroxy-3,4-dihydroquinolin-2(1H)-one 
• 865626-98-8 3-(1-benzylpiperidin-4-yl)quinolin-2(1H)-one 
• 912463-38-8 4-nitrophenyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate 
• 1458062-06-0 (±)-1-(7-benzyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate 
• 1458062-08-2 (±)-1-(7-benzyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)-2-(7-methyl-1H-indazol-5-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate 

Relevant articles and documents

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Synthesis and Pharmacology of Site-Specific Cocaine Abuse Treatment Agents: The Role of the Phenyl Group in Highly Modified Methylphenidate analogs as Dopamine Uptake Inhibitors

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