148759-41-5

Usage

Belongs to the class of amines

It is a compound containing nitrogen atoms that are bonded to carbon atoms, giving it the properties of an amine.

Contains an azide functional group

The presence of the azide group (-N3) gives 1-Pentanamine, 5-azido- its unique properties and reactivity.

Used in organic synthesis and chemical research

1-Pentanamine, 5-azidois used as a building block for the preparation of various compounds and materials.

Potential applications in medicinal chemistry and pharmaceutical research

The azide group in 1-Pentanamine, 5-azido- can be used in click chemistry reactions to facilitate the synthesis of biologically active molecules.

Used in the production of polymers and materials with specific properties and functionalities

1-Pentanamine, 5-azidois used to produce materials with specific properties, such as polymers with azide functional groups.

Upstream product

• 17607-21-5 1,5-diazidopentane 
• 603-35-0 triphenylphosphine 

Downstream Products

• 1224434-30-3 N-((1-(2-aminoethyl)-1H-1,2,3-triazol-4-yl)methyl)-2-(4-(trifluoromethyl)phenyl)diazenecarboxamide 
• 1224434-33-6 N-((1-(3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)-2-(4-(trifluoromethyl)phenyl)diazenecarboxamide 
• 1224434-34-7 N-((1-(4-aminobutyl)-1H-1,2,3-triazol-4-yl)methyl)-2-(4-(trifluoromethyl)phenyl)diazenecarboxamide 
• 1224434-35-8 N-((1-(5-aminopentyl)-1H-1,2,3-triazol-4-yl)methyl)-2-(4-(trifluoromethyl)phenyl)diazenecarboxamide 
• 115416-38-1 N-(5-aminopentyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazole-4-yl)pentanamide 
• 1223077-76-6 (5R,11aS)-2-(5-azidopentyl)-5-(3-benzoyloxyphenyl)-6H-1,2,3,5,11,11a-hexahydroimidazo[1,5-b]-β-carboline-1,3-dione 
• 18807-74-4 N-benzyloxycarbonyl-1,5-pentanediamine hydrochloride 

Relevant academic research and scientific papers

Cucurbit[6]uril as a potential catalyst for the acidic decomposition of azidoaminoalkanes

Five azidoalkyl-1-amines and p-azidoaniline have been synthesized and complexed with cucurbit[6]uril in acidic solutions. Isothermal titration calorimetry has been employed to determine the association constant K and the enthalpy of complex formation ΔH of the azidoalkyl- and azidoarylamines. 4-Azidobutyl-1-amine forms by far the most stable complex. Cucurbit[6]uril significantly catalyzes the decomposition of the azidoalkyl- and azidoarylamines studied.