288089-52-1

Usage

Properties

Contains a pyrrole ring with three methyl groups and a carbaldehyde functional group

Usage

Building block in organic synthesis, flavoring agent in the food industry, manufacturing of pharmaceuticals, fragrance in perfumes and cosmetics

Specific content

Strong odor, potential applications in material science and as a precursor to various other chemical compounds

Upstream product

• 135636-66-7 butane-2,3-dione mono-oxime 
• 64-17-5 ethanol 
• 2199-54-4 2,4,5-trimethyl-3-ethoxycarbonylpyrrole 
• 917-54-4 methyllithium 
• 403815-71-4 3-amino-1-trimethylsilylbut-2-en-1-one 
• 2199-41-9 2,3,5-trimethylpyrrole 
• 68-12-2 N,N-dimethyl-formamide 
• 74-90-8 hydrogen cyanide 

Relevant academic research and scientific papers

Synthesis of silylated β-enaminones and applications to the synthesis of silyl heterocycles

Silyl β-enaminones have been synthesized by reductive cleavage of silylisoxazoles. These versatile synthons bearing the silyl group in different positions of the enamino ketonic system are of great interest in the construction of a variety of penta- and hexaheterocycles, which, in general, retain the silyl group attached at the ring or in a side chain.

Synthesis and physicochemical properties of hydrobromides of alkyl-substituted dipyrrolylmethenes

Hydrobromides of [(alkylpyrrol-2(1H)-ylidenio)methyl]pyrroles (α,α-dipyrrolylmethenes) and of their α,β and β,β isomers were prepared, and their resistance to oxidative thermal degradation was studied. The solvation properties of these compounds in various organic solvents were examined spectrophotometrically and calorimetrically.