6201-69-0

Usage

Chemical composition

Consists of two 4-chloroaniline groups and two chlorine atoms attached to a quinone ring.

Type of compound

Aromatic compound.

Usage

Employed in the production of dyes and pigments.

Applications

Utilized in manufacturing colorants for textiles, plastics, and printing inks.

Molecular structure

Designed to create a range of vibrant and long-lasting colors.

Importance

A valuable ingredient in the formulation of dyes and pigments for various products.

Precaution

Potential health and environmental hazards require careful handling.

InChI:InChI=1/C18H10Cl4N2O2/c19-9-1-5-11(6-2-9)23-15-13(21)18(26)16(14(22)17(15)25)24-12-7-3-10(20)4-8-12/h1-8,23-24H

Upstream product

• 15486-62-1 4-chloro-N-(4-dimethylaminobenzylidene)aniline 
• 118-75-2 chloranil 
• 106-47-8 4-chloro-aniline 
• 95-51-2 o-chloroaniline 
• 904-70-1 N,N'-(1,4-phenylenebis(methan-1-yl-1-ylidene))bis(4-chloroaniline) 

Relevant academic research and scientific papers

Microwave-assisted solvent-free synthesis of some bio-active substituted dihalo 1,4-benzoquinones on silica gel solid support

An environmentally benign solvent-free microwave-assisted synthesis of biologically active 2,5-diarylamino-3,6-dihalo-l,4-benzoquinones by the condensation of substituted anilines and chloranil has been reported on the inorganic solid support of silica ge

An efficient synthesis and biological activity of substituted p-benzoquinones

An efficient synthesis of 2,5-diarylamino-3,6-dichloro-1,4-benzoquinone derivatives has been achieved by condensing mono substituted anilines with tetrachloro-p-benzoquinone in presence of fused sodium acetate as condensing agent under microwave irradiati

A new synthesis of quinoxaline, imidazolidine, indole and carbazole derivatives

Reactions of bis-benzalethylenediamine (1), N,N'-bis(aryl)- and N,N'-bis(cyclohexyl)ethane-1,2-diylidenediamines as well as N,N'-bis(aryl)benzene-1,4-diyldimethylidenediamines 2 with benzo- and naphthoquinones as well as α,β-unsaturated ketones such as 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ); 2,3,5,6-tetrachloro-1,4-benzoquinone (CHl-p); 3,4,5,6-tetrachloro-1,2-benzoquinone (CHl-o); 2,3-dichloro-1,4-naphthoquinone (DCNQ); 2,3-dicyano- l,4-naphthoquinone (DCNQ) and dicyanomethyleneindane-1,3-dione (CNIND) afforded quinoxaline, pyrazinoquinoxaline, imidazolidine, indole and carbazole derivatives as well as arylaminobenzo-, and napthoquinones.

Reaction of Amidine Phenylogous with p-Benzoquinones

N-(4-Dimethylaminobenzylidene)anilines and N1-(4-dimethylaminophenyl)-N1,N2-diphenylformamidine reacted with tetrachloro-, tetrabromo-, and tetrafluoro-p-benzoquinones via charge-transfer complexes formation giving 2-monoa

NEW SYNTHESIS OF TRIPHENODITHIAZINES AND TRIPHENODITHIAZINEQUINOES.

A new class of 6,13-bis(arylamino)triphenodithiazines has been synthesized by condensing chloranil with arylamines followed by the reaction of the resulting 2,5-bis(arylamino)-3,6-dichloro-1,4-benzoquinones with zinc 2-aminobenzenthiolates in the presence