23795-47-3

Usage

Chemical Class

Acrylamides

Structure

It is a derivative of 4-chlorophenyl and contains a cyano and methyl group.

Applications

Potential applications in pharmaceuticals, agriculture, and materials science.

Caution

Handle with caution due to potential toxicity and reactivity.

Safety Protocols

Follow proper safety protocols when handling this chemical.

Further Research

Additional research and testing may be necessary to fully understand its properties and potential uses.

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 6330-25-2 N-methyl-2-cyanoacetamide 

Downstream Products

• 1384177-98-3 2-methyl-1,3-dioxo-5-(4-chlorophenyl)-2-azaspiro[5.5]undecane-4-carbonitrile 

Relevant academic research and scientific papers

One-pot synthesis of functionalized pyrazolo[3,4-c]pyrazoles by reaction of 2-cyano-N-methyl-acrylamide, aryl aldehyde, and hydrazine hydrate

A simple and efficient procedure for the synthesis of novel 4-aryl pyrazolo[3,4-c]pyrazol-3(2H)-ones via a one-pot, three-component reaction between 2-cyano-N-methylacetamide, aryl aldehydes, and hydrazine hydrate in the presence of Et3N in DMF is reported. Products are obtained in good yields and their structures are supported by their spectroscopic data and combustion analysis.

Reaction of 3-aryl-2-cyanothioacrylamides with dimethyl acetylenecarboxylate, methyl propiolate, and N-phenylmaleimide

The reaction of cyanothioacrylamides with dimethyl acetylenedicarboxylate, methyl propiolate, and N-phenylmaleimide was studied. The reaction follows a cycloaddition pathway to give thiopyrans, irrespective of the electronic or spatial effects of the substituents in the thioamide group and in position 3 of the 1-thiabuta-1,3-diene system. The reaction is regio-and stereoselective.