94360-57-3

Usage

Chemical Structure

A cyclopropane ring with two carbon atoms and two nitrogen atoms, a benzoyl group, and a 2,4-dichlorophenyl group.

Functional Groups

Contains a cyclopropane ring, two nitrile groups, a benzoyl group, and a 2,4-dichlorophenyl group.

Reactivity

Versatile reactivity due to the presence of multiple functional groups.

Pharmaceutical Synthesis

Used as an intermediate in the synthesis of various pharmaceuticals.

Agrochemical Synthesis

Utilized in the synthesis of pesticides and herbicides.

Medicinal Chemistry

Potential applications in the development of new drugs for various diseases.

Agricultural Science

Ability to disrupt biological processes in target organisms, making it useful for creating pesticides and herbicides.

Molecular Weight

Approximately 327.18 g/mol (calculated from the chemical formula).

Physical State

Likely a solid at room temperature, due to the presence of a rigid cyclopropane ring and multiple functional groups.

Solubility

May be soluble in organic solvents such as dichloromethane, acetone, or ethanol, due to its nonpolar and polar functional groups.

Upstream product

• 22966-15-0 3-(2,4-dichlorophenyl)-1-phenylprop-2-en-1-one 
• 1885-22-9 bromomalononitrile 
• 94360-14-2 2-Bromo-2-[1-(2,4-dichloro-phenyl)-3-oxo-3-phenyl-propyl]-malononitrile 
• 2972-76-1 2-(2,4-dichlorobenzylidene)malononitrile 
• 70-11-1 α-bromoacetophenone 
• 94360-04-0 2-[1-(2,4-Dichloro-phenyl)-3-oxo-3-phenyl-propyl]-malononitrile 

Relevant academic research and scientific papers

One-pot method for stereoselective cyclopropanation of electron-deficient olefins with methyl bromoacetate and phenacyl bromide in the presence of triphenylarsine

A triphenylarsine-catalyzed one-pot procedure for the preparation of cis-cyclopropanes with acyclic electron-deficient olefins with carbonyl-stabilized arsonium ylides formed from methyl bromoacetate or phenacyl bromide in the presence of NaHCO3/sub

CYCLIZATION OF NITRILES. IX. SYNTHESES BASED ON 2-ARYL-3-AROYL-1,1-DICYANOPROPANES

2-Aryl-3-aroyl-1,1-dicyanopropanes and 2-aryl-3-aroyl-1-bromo-1,1-dicyanopropanes were synthesized from chalcones and malononitrile and were converted into 4,6-diaryl-2-bromo-3-cyanopyridines and 3-cyano-2(1H)-pyridinethiones.The 2-aryl-3-aroyl-1-bromo-1,1-dicyanopropanes proved convenient intermediates for the production of the corresponding cyclopropanes and other compounds.By their reaction with urea a new method was developed for the production of substituted 3-cyano-2(1H)-pyridinethiones.The 2-bromo-3-cyanopyridines contain a mobile bromine atom readily exchanged for the various nucleophilic residues of alcohols and amines and for iodide, and cyano and thiocyanato groups.The 3-cyano-2(1H)-pyridinethiones were used in the synthesis of 3-aminothienopyridines through the isolated 2-Z-methylthio-3-cyanopyridines.