5030-67-1

Usage

General Description

2,5-dichloro-3,6-bis(phenylamino)cyclohexa-2,5-diene-1,4-dione is an organic compound with the molecular formula C18H12Cl2N2O2. It is a synthetic chemical that is primarily used in the manufacturing of dyes and pigments. The compound is known for its deep purple color and is often used in the production of colorants for textiles, plastics, and other materials. Additionally, it has been studied for its potential use in photochemical systems and as a reactive intermediate in organic synthesis. However,

InChI:InChI=1/C18H12Cl2N2O2/c19-13-15(21-11-7-3-1-4-8-11)17(23)14(20)16(18(13)24)22-12-9-5-2-6-10-12/h1-10,21-22H

Upstream product

• 118-75-2 chloranil 
• 62-53-3 aniline 
• 26157-96-0 2,5-Diazido-3,6-dichlor-1,4-benzochinon 
• 22988-31-4 2,5-dichloro-3,6-diphenoxy-[1,4]benzoquinone 
• 33876-90-3 anilino-trichloro-[1,4]benzoquinone 
• 7647-01-0 hydrogenchloride 
• 615-93-0 2,5-Dichloro-1,4-benzoquinone 
• 64-19-7 acetic acid 
• 64-17-5 ethanol 
• 7474-87-5 3,6-Dichlor-2,5-diacetoxy-benzochinon-(1,4) 
• 889-37-2 N,N-dimethyl-4-((phenylimino)methyl)aniline 
• 95794-15-3 N¹-<4-(N,N-dimethylamino)phenyl>-N¹,N²-diphenylformamidine 
• 634-85-5 2,3,6-trichloro-1,4-benzoquinone 
• 101716-14-7 2,5-dianilino-3,6-dichloro-hydroquinone 

Downstream Products

• 6486-69-7 3,10-dichloro-7H,14H-triphenodithiazine-6,13-dione 
• 101716-14-7 2,5-dianilino-3,6-dichloro-hydroquinone 
• 10114-36-0 2,5-dianilino-3,6-dimercapto-[1,4]benzoquinone 
• 4794-44-9 6,13-dichlorotriphenodioxazine 

Relevant academic research and scientific papers

Electronic effects of ligand substitution on spin crossover in a series of diiminoquinonoid-bridged feii2 complexes

A series of four isostructural FeII2 complexes, [(TPyA)2Fe2(XL)]2+ (TPyA = tris(2-pyridylmethyl)amine; XL2- = doubly deprotonated form of 3,6-disubstituted-2,5-dianili

Electronic effects of ligand substitution on spin crossover in a series of diiminoquinonoid-bridged FeII2 complexes

A series of four isostructural FeII2 complexes, [(TPyA)2Fe2(XL)]2+ (TPyA = tris(2-pyridylmethyl)amine; XL2-= doubly deprotonated form of 3,6-disubstituted-2,5-dianilin

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

Synthesis of indolocarbazole quinones; potent aryl hydrocarbon receptor ligands

Syntheses of indolo[2,3-b]carbazole-6,12-dione and the isomeric indolo[3,2-b]carbazole-6,12-dione, an extremely efficient inducer of the aryl hydrocarbon (Ah) receptor are described. Initial oxidation of the parent indolo[3,2-b]carbazole followed by sever

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