120811-06-5

Usage

Molecular structure

Contains a pyrano-pyridine core with two carbonitrile groups, an acetyl group, an amino group, and two methoxyphenyl groups

Potential applications

Pharmaceuticals and materials science

Unique structural features

Complex molecular structure with multiple functional groups

Potential biological activities

Further research needed to fully understand properties and uses of this chemical.

Upstream product

• 2826-26-8 2-(4-methoxyphenylmethylene)malononitrile 
• 105263-07-8 5-acetyl-2-amino-6-methyl-4-(4-methoxy-phenyl)-4H-pyran-3-carbonitrile 
• 123-54-6 acetylacetone 
• 15725-17-4 3-(4-methoxybenzylidene)-2,4-pentanedione 
• 109-77-3 malononitrile 

Relevant academic research and scientific papers

REACTIONS OF SIX-MEMBERED HETEROCYCLIC β-ENAMINONITRILES WITH ELECTROPHILIC REAGENTS

The nitriles I reacted with acetylacetone and with ethyl acetoacetate to afford 2-amino-3-cyano-4H-pyran derivatives.They reacted further to yield pyranopyridine derivatives.The reaction of V with acetylacetone afforded the pyridinethione VIII.This afford

Nitriles in Organic Synthesis: The Reaction of Cinnamonitriles with Cyclohexanone and Acetylacetone

The reaction of 1a,b with cyclohexanone afforded hexahydronaphthalene derivatives (3a,b).In contrast to the behaviour of 1a,b, cyclohexanone reacts with 4a-c to yield the propenylidenecyclohexanone derivatives (5a-c).The reaction of 1a with acetylacetone

A CONVENIENT, ONE STEP SYNTHESIS OF PYRANOPYRIDINES

A novel one step synthesis of pyranopyridines from malononitrile and unsaturated ketones is reported.The reaction mechanism is discussed and takes place through an intermediate monocyclic 4H-pyran.Several derivatives with different substitution pat