31604-30-5

Basic information

• Product Name: 1,2,4,5-TETRABROMO-3,6-DICHLORO-BENZENE
• Synonyms: 1,2,4,5-TETRABROMO-3,6-DICHLORO-BENZENE
• CAS NO: 31604-30-5
• Molecular Formula: C₆Br₄Cl₂
• Molecular Weight: 462.5862
• Mol File: 31604-30-5.mol
• Article Data: 7

Chemical Properties

• Melting Point: 281 °C
• Boiling Point: 394.0±37.0 °C(Predicted)
• Appearance: /
• Density: 2.597±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1,2,4,5-TETRABROMO-3,6-DICHLORO-BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4,5-TETRABROMO-3,6-DICHLORO-BENZENE(31604-30-5)
• EPA Substance Registry System: 1,2,4,5-TETRABROMO-3,6-DICHLORO-BENZENE(31604-30-5)

Safety Data

• Hazardous Substances Data: 31604-30-5(Hazardous Substances Data)

Usage

General Description

1,2,4,5-Tetrabromo-3,6-dichloro-benzene is a chemical compound used as a flame retardant and pesticide. It is a colorless to white crystalline solid that is insoluble in water. 1,2,4,5-TETRABROMO-3,6-DICHLORO-BENZENE is known to be highly persistent in the environment, with a very long half-life and potential for bioaccumulation in aquatic organisms. It is considered to be toxic to aquatic life and is classified as a persistent organic pollutant. Exposure to this chemical has been linked to harmful effects on the liver, kidneys, and reproductive system in animal studies. Due to its potential environmental and health risks, there are regulations in place to limit its use and release into the environment.

Upstream product

• 106-46-7 para-dichlorobenzene 
• 53628-88-9 2-tert-butyl-1,4-dichloro-benzene 
• 89244-49-5 C₆Br₂Cl₂Li₂ 

Downstream Products

• 25634-86-0 1,2,4,5-tetrakis(styryl)benzene 
• 4571-24-8 2,5-dibromo-1,4-dichlorobenzene 
• 3383-32-2 1,2,4,5-tetraphenylbenzol 
• 73557-61-6 1,3,4-tribromo-2,5-dichlorobenzene 
• 89244-51-9 1,4-Dibromo-2,5-dichloro-3,6-diiodo-benzene 
• 89244-53-1 1-(4-Acetyl-2,5-dibromo-3,6-dichloro-phenyl)-ethanone 
• 1967-89-1 1,4-dichlorodurene 
• 89244-52-0 1,4-dibromo-2,5-dichloro-3,6-dimethyl-benzene 
• 89244-54-2 1,4-Dibromo-2,5-dichloro-3,6-bis-phenylsulfanyl-benzene 
• 89244-55-3 [2,5-Dibromo-3,6-dichloro-4-(hydroxy-phenyl-methyl)-phenyl]-phenyl-methanol 

Relevant articles and documents

The regioselective generation of arynes from polyhalogenobenzenes. An improved synthesis of syn- and anti-1,4,5,8,9,12-hexahydro-1,4:5,8:9,12-triepoxytriphenylene

The halogenated benzenes, 1,2,4,5-tetrabromobenzene 6, hexabromobenzene 9, p-dichlorotetrabromobenzene 11, and 1,2-dibromo-4,5-dichlorobenzene 12, were investigated as 1,3-bis-, 1,4-bis-, and 1,3,5-tris-aryne precursors by using alkyllithiums and alkali m

A novel graphite-like stacking structure in a discrete molecule and its molecular recognition behavior

A graphite-like stacking structure was nicely reproduced in a discrete molecule that was prepared by 2+2 macrocyclic Schiff base formation. In the crystal structure, two hexabenzocoronene planes are closely stacked with displacement, yielding the intramolecular stacking structure similar to an AB- or ABC-stacking pattern in natural graphite. This molecule showed a recognition ability toward electron-deficient aromatic molecules in solution.

PERBROMINATION OF BENZENE AND SOME OF ITS DERIVATIVES

Perbrominated compounds - pentabromophenol, hexabromobenzene, pentabromotoluene, polychlorobromobenzenes, and decabromodiphenyl ether - have been obtained.Substitution bromination has been discovered in treating diphenyl sulfoxide, diphenyl sulfide, diphenylmethane, diphenyl oxide, and benzophenone with excess bromine in the presence of AlBr3.A series of ethers and esters of pentabromophenol have been obtained; their hydrolysis has been carried out.A negative influence of ferric halides has been discovered in exhaustive bromination of aromatic compounds.