76272-58-7

Basic information

• Product Name: 9-Azabicyclo[3.3.1]nonan-3-amine, 9-(phenylmethyl)-, endo-
• CAS NO: 76272-58-7
• Molecular Formula: C15H22N2
• Molecular Weight: 230.353
• Mol File: 76272-58-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 9-Azabicyclo[3.3.1]nonan-3-amine, 9-(phenylmethyl)-, endo-(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Azabicyclo[3.3.1]nonan-3-amine, 9-(phenylmethyl)-, endo-(76272-58-7)
• EPA Substance Registry System: 9-Azabicyclo[3.3.1]nonan-3-amine, 9-(phenylmethyl)-, endo-(76272-58-7)

Safety Data

• Hazardous Substances Data: 76272-58-7(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 111-30-8 Glutaraldehyde 

Downstream Products

• 142894-64-2 1-Methyl-1H-indole-3-carboxylic acid ((1R,3R,5S)-9-benzyl-9-aza-bicyclo[3.3.1]non-3-yl)-amide 
• 1210745-16-6 N-[(3-endo)-9-(phenylmethyl)-9-azabicyclo[3.3.1]non-3-yl]-1H-indazole-3-carboxamide 
• 1394134-30-5 tert-butyl (S,E)-8-(9-benzyl-9-azabicyclo[3.3.1]nonan-3-ylamino)-2-methyl-8-oxooct-5-en-4-ylcarbamate 
• 153431-10-8 3β-<(tert-butyloxycarbonyl)amino>-9-benzyl-9-azabicyclo<3.3.1>nonane 
• 155560-04-6 tert-butyl-9-azabicyclo[3.3.1]nonan-3-ylcarbamate 
• 160177-67-3 endo-N-(9-azabicyclo[3.3.1]non-3-yl)-1-methyl-1H-indazole-3-carboxamide 
• 128395-47-1 1-methyl-N-[(3-endo)-9-(phenylmethyl)-9-azabicyclo[3.3.1]non-3-yl]-1H-indazole-3-carboxamide 
• 142894-63-1 1H-Indole-3-carboxylic acid ((1R,3R,5S)-9-benzyl-9-aza-bicyclo[3.3.1]non-3-yl)-amide 

Relevant articles and documents

Predicting Electrocatalytic Properties: Modeling Structure-Activity Relationships of Nitroxyl Radicals

Stable nitroxyl radical-containing compounds, such as 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) and its derivatives, are capable of electrocatalytically oxidizing a wide range of alcohols under mild and environmentally friendly conditions. Herein, we examine the structure-function relationships that determine the catalytic activity of a diverse range of water-soluble nitroxyl radical compounds. A strong correlation is described between the difference in the electrochemical oxidation potentials of a compound and its electrocatalytic activity. Additionally, we construct a simple computational model that is able to accurately predict the electrochemical potential and catalytic activity of a wide range of nitroxyl radical derivatives.

Toward biophysical probes for the 5-HT3 receptor: Structure-activity relationship study of granisetron derivatives

This report describes the synthesis and biological characterization of novel granisetron derivatives that are antagonists of the human serotonin (5-HT3A) receptor. Some of these substituted granisetron derivatives showed low nanomolar binding affinity and allowed the identification of positions on the granisetron core that might be used as attachment points for biophysical tags. A BODIPY fluorophore was appended to one such position and specifically bound to 5-HT3A receptors in mammalian cells.

Azabicyclo[3.2.1]octan-3α-yl and azabicyclo[3.3.1]nonan-3α-yl carbamates as σ2-selective radiotracers

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