718-16-1

Usage

Chemical structure

The compound consists of a butanamine molecule with a nitrophenylmethylene group attached to the nitrogen atom.

Classification

It is an organic compound.

Potential applications

The compound has potential applications in various industries, including pharmaceuticals, agriculture, and manufacturing.

Use as a reagent

Due to its unique structure and properties, it is suitable for use as a reagent in chemical reactions.

Use as an intermediate

It can be used as an intermediate in the synthesis of complex organic molecules.

Use as a building block

The compound can serve as a building block for creating more complex chemical structures.

Biological activity

It may have potential biological activity, which could be investigated for its potential use in medicinal or agrochemical applications.

Versatility

1-Butanamine, N-[(3-nitrophenyl)methylene]is a versatile chemical compound with various potential applications in different fields.

Upstream product

• 99-61-6 3-nitro-benzaldehyde 
• 109-73-9 N-butylamine 

Downstream Products

• 132784-76-0 1-nitro-3-(2-chloro-2-nitroethenyl)benzene 
• 1353055-50-1 N-(3-nitrobenzylidene)-1H-imidazol-2-amine 
• 62498-74-2 N-(3-nitrobenzyl)butan-1-amine 
• 95866-25-4 4-(3-nitro-phenyl)-isoxazole-3,5-dicarboxylic acid bis-butylamide 

Relevant academic research and scientific papers

Dipicolylamine coupled rhodamine dyes: New clefts for highly selective naked eye sensing of Cu2+ and CN- ions

The dipicolylamine (DPA) motif which is known as a binder of Zn(ii) ions, has been utilized in devising rhodamine labelled compounds 1 and 2. Compound 1 acts as a FRET sensor and shows excellent selectivity for Cu(ii) ions over a series of other cations in CH3CN/H2O by exhibiting a colour change (colourless to pink) of the solution. The spectral and colour changes are recovered in the presence of CN- ions and thus, the ensemble 1·Cu2+ in CH3CN/H2O is established as the medium for selective detection of CN- ions. In contrast, the modified compound 2 with the dipicolylamine motif as the principal binding site has been established as the colorimetric sensor of Cu(ii) ions and the fluorometric sensor of Hg(ii), Zn(ii) and Cd(ii) ions. Both the compounds 1 and 2 are cell permeable and are successfully employed for the detection of intercellular metal ions through bright field and fluorescence imaging.

A new protocol for a one-pot synthesis of α-amino phosphonates by reaction of imines prepared in situ with trialkylphosphites

Imines prepared in situ by reaction of aldehydes and ketones with primary amines in ethereal solution of LiClO4 react readily at ambient temperature with trialkylphosphite to give high yields of α-amino phosphonates.