27761-50-8

Usage

Chemical structure

Contains a phenylhydrazono group attached to the anthracen-9(10H)-one molecule
The phenylhydrazono group is a functional group derived from phenylhydrazine, which is attached to the anthracen-9(10H)-one, a tricyclic aromatic ketone.

Classification

Organic compound
It is a compound primarily containing carbon and hydrogen atoms, along with other elements such as nitrogen and oxygen.

Appearance

Yellow crystalline
The compound has a yellow color and forms a crystalline solid.

Solubility

Insoluble in water, soluble in organic solvents
It does not dissolve in water but can dissolve in organic solvents like alcohols, ethers, and hydrocarbons.

Applications

Organic synthesis, reagent in chemical reactions, pharmaceuticals, dyes, and chemical intermediates
The compound is used in various chemical processes, including the synthesis of other organic compounds, as a reagent in chemical reactions, and in the production of pharmaceuticals, dyes, and other industrial chemicals.

Potential uses

Research and development in various industries
Due to its unique chemical properties, the compound may have potential applications in research and development across different industries, such as pharmaceuticals, materials science, and chemical manufacturing.

Upstream product

• 21555-13-5 10,10-dibromoanthrone 
• 100-63-0 phenylhydrazine 
• 1560-32-3 10-bromo-10H-anthracen-9-one 
• 71-43-2 benzene 
• 2684-02-8 benzenediazonium 
• 64-17-5 ethanol 
• 90-44-8 anthracen-9(10H)-one 
• 62-53-3 aniline 
• 529-86-2 9-anthrol 
• 64-19-7 acetic acid 

Downstream Products

• 619-97-6 benzenediazonium nitrate 
• 84-65-1 9,10-phenanthrenequinone 
• 100-63-0 phenylhydrazine 

Relevant academic research and scientific papers

Phenylimino-10H-anthracen-9-ones as novel antimicrotubule agents - Synthesis, antiproliferative activity and inhibition of tubulin polymerization

A novel series of phenylimino-10H-anthracen-9-ones and 9-(phenylhydrazone)- 9,10-anthracenediones were synthesized and evaluated for interaction with tubulin and for cytotoxicity against a panel of human tumor cell lines. The 10-(3-hydroxy-4-methoxy-pheny

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.

Reactions of Aromatic Nitro Compounds. LXX. Formation of 10-Alkoxy-9-Nitro-9-Arylazo-9,10-dihydroanthracenes and 9,10-Anthraquinone Arylhydrazones in the Reaction of 9-Nitroanthracene Anionic σ-Complexes with Aromatic Diazo Compounds

Reaction of 9-nitroanthracene anionic σ complexes with potassium alkoxides (CH3OK, C2H5OK) and substituted aryldiazonium tetrafluoroborates [RC6H4N2+BF4-, R