5030-67-1

Basic information

• Product Name: 2,5-dichloro-3,6-bis(phenylamino)cyclohexa-2,5-diene-1,4-dione
• Synonyms: 2,5-dichloro-3,6-bis(phenylamino)cyclohexa-2,5-diene-1,4-dione;2,5-Dianilino-3,6-dichloro-p-benzoquinone;C.I.56010;C.I.Vat Brown 24;C.I.Vat Brown 34
• CAS NO: 5030-67-1
• Molecular Formula: C₁₈H₁₂Cl₂N₂O₂
• Molecular Weight: 359.20608
• Mol File: 5030-67-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 472.8°Cat760mmHg
• Flash Point: 239.7°C
• Appearance: /
• Density: 1.44g/cm³
• Vapor Pressure: 4.16E-09mmHg at 25°C
• Refractive Index: 1.677
• CAS DataBase Reference: 2,5-dichloro-3,6-bis(phenylamino)cyclohexa-2,5-diene-1,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-dichloro-3,6-bis(phenylamino)cyclohexa-2,5-diene-1,4-dione(5030-67-1)
• EPA Substance Registry System: 2,5-dichloro-3,6-bis(phenylamino)cyclohexa-2,5-diene-1,4-dione(5030-67-1)

Safety Data

• Hazardous Substances Data: 5030-67-1(Hazardous Substances Data)

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

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

Downstream Products

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

Relevant articles and documents

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

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

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