6937-78-6

Usage

Uses

Used in Organic Synthesis:
9,10-dioxo-9,10-dihydroanthracene-1,4-dicarbonyl dichloride is used as a key intermediate in organic synthesis for the production of dyes and pigments. Its unique structure and reactivity make it a valuable component in creating a variety of colorants for different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 9,10-dioxo-9,10-dihydroanthracene-1,4-dicarbonyl dichloride serves as a precursor for the preparation of various drugs. Its versatility in chemical reactions allows for the development of new pharmaceutical compounds with potential therapeutic benefits.
Used in Agrochemical Industry:
9,10-dioxo-9,10-dihydroanthracene-1,4-dicarbonyl dichloride is also utilized as a starting material in the synthesis of agrochemicals. Its role in creating effective pesticides and other agricultural products contributes to enhancing crop protection and yield.
Safety Precautions:
Due to its highly reactive and potentially hazardous nature, 9,10-dioxo-9,10-dihydroanthracene-1,4-dicarbonyl dichloride requires proper safety measures during handling and usage. This includes the use of personal protective equipment, working in well-ventilated areas, and following established safety protocols to minimize risks.

Upstream product

• 54292-11-4 9,10-dioxo-9,10-dihydro-1,4-anthracene dicarboxylic acid 
• 1519-36-4 1,4-dimethylanthraquinone 

Downstream Products

• 873981-15-8 9-hydroxy-10-oxo-9-phenyl-9,10-dihydro-anthracene-1,4-dicarboxylic acid 

Relevant academic research and scientific papers

Improved synthesis dimethylhomoecoerdianthrone (HOCD) and its functionalization through facile amination reactions

An improved synthesis of dimethylhomoecoerdianthrone (HOCD), a dye used for singlet oxygen detection, was reported by isolation of a key intermediate followed by cyclization reaction. Moreover, dehydrogenative amination reaction between HOCD and alkyl ami

Dye and fluorescent probe for detecting singlet oxygen and manufacturing method of dye and fluorescent probe

The application discloses a synthetic method of a dye compound used for sensitive detection of singlet oxygen. Furthermore, a fluorescent probe having a part of different fluorescent groups of the dye compound is designed and is synthesized through a new

Synthesis of new polycyclic anthracenedione analogs with hetero- Or carbocyclic ring(s) fused to the chromophore system

A series of novel anthracenedione analogs with various hetero- or carbocyclic ring(s) incorporated into the chromophore has been synthesized. These compounds may constitute a new class of anthracenedione agents with potential ability to overcome multidrug resistance of cancer cells.

1,4-disubstituted anthracene antitumor agents

Three different types of 1,4-disubstituted anthracenes were synthesized, and their cytotoxicity in a panel of tumor cells was compared with that of the corresponding 9,10-disubstituted anthracenes. The panel contained human myeloma, melanoma, colon, and lung cancer cells and sensitive and multidrug- resistant murine L1210 leukemia cells. These compounds had [[(dimethylamino)ethyl]amino]methyl, N-[(dimethylamino)ethyl]carbamoyl, and carboxaldehyde (4,5-dihydro-1H-imidazol-2-yl)hydrazone side chains. The 1,4- diamide was more potent across the tumor panel than the corresponding 9,10- isomer, but the 1,4-diamine and the 1,4-hydrazone were less potent than their 9,10-isomers. Although the 1,4-hydrazone was active against P388 leukemia in mice, it was inactive against L1210 leukemia. Within each pair of compounds, the one with greater average potency against tumor cells gave a greater increase in the transition melt temperature of DNA.