10395-02-5

Usage

Uses

Used in Organic Synthesis:
(10-oxoanthracen-9(10H)-ylidene)propanedinitrile is used as a building block in organic synthesis for the preparation of various organic molecules. Its unique structure and reactivity allow for the creation of a wide range of compounds with diverse properties and applications.
Used in Organic Electronics:
(10-oxoanthracen-9(10H)-ylidene)propanedinitrile is used in the field of organic electronics due to its potential applications in the development of new materials and devices. Its chemical properties and reactivity make it a promising candidate for use in organic solar cells, light-emitting diodes, and other electronic components.
Used in Materials Science:
In materials science, (10-oxoanthracen-9(10H)-ylidene)propanedinitrile is used for the development of new materials with specific properties. Its unique structure and chemical properties contribute to the creation of materials with improved performance in various applications, such as coatings, adhesives, and composites.
Used in Pharmaceutical Production:
(10-oxoanthracen-9(10H)-ylidene)propanedinitrile is used as an intermediate in the production of pharmaceuticals. Its chemical properties and reactivity make it a valuable component in the synthesis of various drugs, contributing to the development of new treatments and therapies.
Used in Dye Production:
(10-oxoanthracen-9(10H)-ylidene)propanedinitrile is also used in the production of dyes, where its unique structure and chemical properties contribute to the development of dyes with specific color characteristics and properties. (10-oxoanthracen-9(10H)-ylidene)propanedinitrile plays a crucial role in the creation of dyes for various industries, including textiles, printing, and cosmetics.

Upstream product

• 84-65-1 9,10-phenanthrenequinone 
• 109-77-3 malononitrile 
• 90-44-8 anthracen-9(10H)-one 
• 156755-16-7 10-(dicyanomethylidene)-9(10H)-anthrone hydrazone 

Relevant academic research and scientific papers

On the Chemical Nature of 10-Dicyanomethyleneanthrone Hydrazone

The chemical nature of 10-dicyanomethylene-9-anthrone hydrazone was examined.It was shown that this compound bearing the conjugated ylidenemalononitrile fragment and hydrazonic moiety did not undergo transformations characteristic of ylidenemalononitriles, e.g., reduction and Michael addition, but possesses properties typical for hydrazones.Thus it could be hydrolyzed, acetylated, oxidized to yield the diazo compound, and reacted with acetone to form the corresponding azine.These properties were interpreted using semiempirical (AM1) and force field calculations. - Keywords. 10-Dicyanomethylene-9-anthrone hydrazone; 10-Dicyanomethylene-9-anthrone; N-Acetyl-10-dicyanomethylene-9-anthrone hydrazone; (10-dicyanomethylene-9,10-dihydroanthracene-9-ylidene)-isopropylidene-hydrazine; 9-Diazo-10-(dicyanomethylene)-9,10-dihydro anthracene; Acetylation; Oxidation; Hydrolysis; Semiempirical calculations.

Reaction of anthrone and its 1- and 4-substituted derivatives with sulfur in the presence of nucleophiles

Anthrone and its 1-substituted derivatives react with molecular sulfur in the presence of nucleophiles (aromatic amines, hydrazine, substituted hydrazines, and malononitrile) to give intermediate monothioanthraquinones which are then converted into mixtures of the corresponding anthraquinones and 10-imino-, 10-hydrazono-, or 10-dicyanomethylene-9,10-dihydroanthracen-9-ones. Unlike 1-substituted derivatives, 4-substituted anthrones react with sulfur in the presence of phenylhydrazine to give only 1-substituted anthraquinones.

New Electron Acceptors: Synthesis, Electrochemistry, and Radical Anions of N,7,7-Tricyanoquinomethanimines and X-ray Crystal Structures of the Trimethyl and Tetramethyl Derivatives

The reaction of a range of quinones 3 with malononitrile in the presence of titanium tetrachloride/pyridine yields dicyanoquinomethides 4, which on reaction wit N,N'-bis(trimethylsilyl)carbodiimide are converted into the corresponding N,7,7-tricyanoquinom

N,7,7-Tricyanoquinomethaneimines: New Electron Acceptors for Organic Metals

Four derivatives of the title system, which is a new class of electron acceptor, have beensynthesised; cyclic voltammetric data show that these compounds undergo one- and two-electron reductions.