73713-78-7

Usage

Chemical structure

A cyclohexadienedione ring with two chlorine atoms and two morpholine groups attached to it.

Type of compound

Synthetic organic compound.

Potential applications

Pharmaceutical research and organic synthesis.

Unique chemical properties

Presence of chlorine atoms and morpholine groups contribute to the compound's unique reactivity and suitability for various chemical reactions.

Use as a building block

The compound can be used for the synthesis of more complex organic molecules.

Research interest

Researchers and chemists are interested in 2,5-dichloro-3,6-di(morpholin-4-yl)cyclohexa-2,5-diene-1,4-dione due to its structural and functional properties.

Field of study

The compound is a subject of investigation in the field of organic chemistry.

Upstream product

• 110-91-8 morpholine 
• 615-93-0 2,5-Dichloro-1,4-benzoquinone 
• 118-75-2 chloranil 

Relevant academic research and scientific papers

New type of quinone-quinone complexation in the reaction of 2,5-dichloro-1,4-benzoquinone with morpholine at high pressure

The complex of tetrakis(morpholino)-1,4-benzoquinone with 2,5-bis(morpholino)-1,4-benzoquinone of 2:1 stoichiometry was obtained in 9 % yield in the reaction of 2,5-dichloro-1,4-benzoquinone with morpholine at high pressure.

Micelles catalyzed chemo- and regio-selective one pot and one step synthesis of 2,3,5,6-tetrakis(alkyl and arylsulfanyl)-1,4-benzoquinones and 2,5-diaminosubstituted-1,4-benzoquinones "in-Water" and their biological evaluation as antibacterial and antifungal agents

Chemo- and regio-selective one pot and one step synthesis of novel 2,3,5,6-tetrakis (substituted thio)cyclohexa-2,5-diene-1,4-diones (4d-14), 2,5-dichloro-3,6-diaminocyclohexa-2,5-diene-1,4-diones and 2,5-diaminocyclohexa- 2,5-diene-1,4-diones (16) by economical green methodology approach using LD (Laundry detergent) as a catalyst "In-Water" by nucleophilic addition and substitution reactions of 1,4-benzoquinone and chloranil with sulfur and nitrogen nucleophiles in high yields has been demonstrated. The antifungal profile of 4 and 16 indicates that compounds 4d and 16f had better antifungal activity compared to clinically prevalent antifungal drugs Fluconazole, 5-Fluorocytosine and Clotrimazole against Sporothrix schenckii and Trichophyton mentagraphytes. 16f had also been found to possess better antibacterial activity compared to Ampicillin in vitro against Escherichia coli, Staphylococcus aureus and Klebsiella pneumoniae. Compound 16f did not exhibit any toxicity towards mammalian cells L929.