79098-92-3

Basic information

• Product Name: 1-benzyl-4-(2-hydroxyphenylmethyl)aminopiperidine
• Synonyms: 1-benzyl-4-(2-hydroxyphenylmethyl)aminopiperidine
• CAS NO: 79098-92-3
• Molecular Weight: 296.412
• Mol File: 79098-92-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-benzyl-4-(2-hydroxyphenylmethyl)aminopiperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-4-(2-hydroxyphenylmethyl)aminopiperidine(79098-92-3)
• EPA Substance Registry System: 1-benzyl-4-(2-hydroxyphenylmethyl)aminopiperidine(79098-92-3)

Safety Data

• Hazardous Substances Data: 79098-92-3(Hazardous Substances Data)

Upstream product

• 50541-93-0 4-amino-1-benzylpiperidine 
• 90-02-8 salicylaldehyde 
• 1205-72-7 1-benzyl-4-amino-piperidine dihydrochloride 

Downstream Products

• 1347747-05-0 C₂₉H₃₀F₂N₂O₂ 
• 79106-55-1 1-<2-(3,4,5-trimethoxyphenyl)-2-hydroxyethyl>-4-(2-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)piperidine 
• 79106-53-9 threo-1-<2-(3,4-dimethoxyphenyl)-2-hydroxy-1-methyethyl>-4-(2-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)piperidine 
• 79106-54-0 1-(3,4,5-trimethoxybenzoylmethyl)-4-(2-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)piperidine 
• 79106-52-8 1-[1-(3,4-dimethoxybenzoyl)-ethyl]-4-(2-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)-piperidine 
• 79106-50-6 1-[2-(3,4-Dimethoxyphenyl)-2-hydroxyethyl]-4-(2-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)-piperidine 
• 79106-48-2 1-(3,4-dimethoxybenzoylmethyl)-4-(2-oxo-3,4-dihydro-2H-1,3-benzoxazin-3-yl)-piperidine 
• 98767-73-8 3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one 
• 98767-69-2 3-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one 
• 79098-93-4 1-benzyl-4-(2-oxo-3,4-dihydro-2H-1,3-benzoxazine-3-yl)piperidine 

Relevant articles and documents

Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries

Solid supported nucleophiles and electrophiles are employed to expedite the work-up and purification of a variety of amine alkylations and acylations. These solid supported scavengers are particularly advantageous for the construction of non-peptide libraries in a parallel array format.

DIPHENYLBUTYPIPERIDINE AUTOPHAGY INDUCERS

Autophagy inducing compounds, methods of their preparation and use, and kits containg said compounds are disclosed herein.

Piperidine derivatives

New piperidine derivatives which have a useful pharmacological activity such as hypotensive activity are prepared.