113445-83-3

Basic information

• Product Name: 1-{2-[(4-tert-Butoxycarbonylamino-phenyl)-methyl-amino]-1-methyl-ethyl}-4-(phenyl-propionyl-amino)-piperidine-4-carboxylic acid methyl ester
• CAS NO: 113445-83-3
• Molecular Weight: 552.714
• Mol File: 113445-83-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-{2-[(4-tert-Butoxycarbonylamino-phenyl)-methyl-amino]-1-methyl-ethyl}-4-(phenyl-propionyl-amino)-piperidine-4-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{2-[(4-tert-Butoxycarbonylamino-phenyl)-methyl-amino]-1-methyl-ethyl}-4-(phenyl-propionyl-amino)-piperidine-4-carboxylic acid methyl ester(113445-83-3)
• EPA Substance Registry System: 1-{2-[(4-tert-Butoxycarbonylamino-phenyl)-methyl-amino]-1-methyl-ethyl}-4-(phenyl-propionyl-amino)-piperidine-4-carboxylic acid methyl ester(113445-83-3)

Safety Data

• Hazardous Substances Data: 113445-83-3(Hazardous Substances Data)

Upstream product

• 72996-78-2 methyl 4-[N-(1-oxopropyl)-N-phenylamino]-4-piperidinecarboxylate 
• 113445-80-0 [4-(2-Oxo-propylamino)-phenyl]-carbamic acid tert-butyl ester 
• 71026-66-9 N-(tert-butoxycarbonyl)-1,4-phenylenediamine 
• 50-00-0 formaldehyd 
• 113445-82-2 1-[2-(4-tert-Butoxycarbonylamino-phenylamino)-1-methyl-ethyl]-4-(phenyl-propionyl-amino)-piperidine-4-carboxylic acid methyl ester 

Downstream Products

• 113445-79-7 4-({2-[4-Methoxycarbonyl-4-(phenyl-propionyl-amino)-piperidin-1-yl]-propyl}-methyl-amino)-benzenediazonium 
• 113445-78-6 1-{2-[(4-Amino-phenyl)-methyl-amino]-1-methyl-ethyl}-4-(phenyl-propionyl-amino)-piperidine-4-carboxylic acid methyl ester 

Relevant articles and documents

MARQUAGE IRREVERSIBLE DES RECEPTEURS DES OPIOIDES A L'AIDE DE SELS D'ARYLDIAZONIUM DERIVES DU FENTANYL

The synthesis of several fentanyl derivatives is reported.The binding affinity of these compounds to membrane opioid receptors is also presented.Several potentially irreversible aryldiazonium ligands were tested for irreversible inactivation of opioid receptors.Compound 13 was shown to inactivate up to 50percent of rat brain opioid receptors, in a ligand-protectable manner.It is therefore a potentially efficient affinity probe for these receptors.