128915-84-4

Basic information

• Product Name: 1,4-DIBROMO-2,5-DI(BUTOXY)BENZENE
• Synonyms: 1,4-DIBROMO-2,5-DI(BUTOXY)BENZENE
• CAS NO: 128915-84-4
• Molecular Formula: C₁₄H₂₀Br₂O₂
• Molecular Weight: 380.12
• Mol File: 128915-84-4.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-DIBROMO-2,5-DI(BUTOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DIBROMO-2,5-DI(BUTOXY)BENZENE(128915-84-4)
• EPA Substance Registry System: 1,4-DIBROMO-2,5-DI(BUTOXY)BENZENE(128915-84-4)

Safety Data

• Hazardous Substances Data: 128915-84-4(Hazardous Substances Data)

Usage

Physical State

Colorless to light yellow liquid

Primary Use

Flame retardant in plastics, textiles, and electronics

Solubility

Insoluble in water, soluble in organic solvents

Environmental Impact

Toxic to aquatic organisms, may cause long-term adverse effects in the environment

Additional Uses

Crosslinking agent in polymer production, building block in synthesis of other organic compounds

Safety Precautions

Handle with caution due to potential environmental and health hazards

Upstream product

• 770747-30-3 (2,5-dibutoxyphenyl)boronic acid 
• 123-31-9 hydroquinone 
• 109-65-9 1-bromo-butane 
• 14753-51-6 2,5-dibromohydroquinone 
• 104-36-9 1,4-dibutoxybenzene 

Downstream Products

• 1262137-07-4 4-bromo-2,5-bis(butoxy)benzaldehyde 
• 128834-29-7 1,4-bis(ethynyl)-2,5-di(butyloxy)benzene 
• 564456-59-3 2,5-bis(butoxy)benzene-1,4-dialdehyde 
• 179264-44-9 1,4-Bis(3-hydroxy-3-methylbut-1-ynyl)-2,5-di-n-butoxybenzene 
• 380626-51-7 1,4-dibutoxy-2,5-bis(thiophen-2-yl)benzene 
• 52251-23-7 1,4-dibutoxy-2,5-dicyanobenzene 
• 907584-46-7 4-(2,5-dibutoxy-4-[2,2';6',2'']terpyridin-4'-ylethynyl-phenyl)-2-methyl-but-3-yn-2-ol 
• 907584-30-9 4'-(2,5-dibutoxy-4-ethynyl-phenylethynyl)-[2,2';6',2'']terpyridine 
• 907584-29-6 4-(2,5-dibutoxy-4-ethynyl-phenyl)-2-methyl-but-3-yn-2-ol 
• 1451053-64-7 2,2'-(2,5-dibutoxy-1,4-phenylene)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane) 
• 1568011-51-7 4-(2,5-bis(butoxy)-4-((E)-2-(pyridin-4-yl)vinyl)styryl)pyridine 
• 1407152-24-2 1,4-dibutoxy-2,5-bis(furan-2-yl)benzene 
• 1407152-25-3 1,4-dibutoxy-2,5-bis(selenophen-2-yl)benzene 
• 52351-58-3 11-Chloro-undecanoic acid 2,5-dibutoxy-4-[(11-chloro-undecanoylamino)-methyl]-benzylamide 

Relevant articles and documents

CONSTRUCTION OF A COBALT COORDINATION POLYMER BASED ON A LINEAR LIGAND WITH FLEXIBLE BRANCHED CHAINS

Abstract: A cobalt coordination polymer based on a linear ligand with flexible branched chains 4,4′-(2,5-dibutoxy-1,4-phenylene)dipyridine (BPDP), namely, {[Co(BPDP)(H2O)4]·2BPDP·2NO3}n, is obtained and characterized by the elemental analysis and single crystal X-ray diffraction. The UV-Visible spectral features are also investigated in details.

Bipyridyl ligand and preparation method thereof, ruthenium supramolecular self-assembly body containing bipyridyl ligand and preparation method and application of ruthenium supramolecular self-assembly

The invention provides a novel bipyridyl bidentate ligand and a preparation method thereof. The structural formula of the novel bipyridyl bidentate ligand is shown in the specification. The inventionfurther provides a ruthenium supramolecular self-assembly body of the ligand and a preparation method of the ruthenium supramolecular self-assembly body. The preparation method comprises the followingsteps: putting a prepared ruthenium receptor and a bipyridyl ligand into a container, adding a mixed solvent of methanol and dichloromethane in equal proportion, stirring for a period of time at roomtemperature, spin-drying the solution to a certain volume after the reaction is finished, slowly adding diethyl ether, and separating out solid powder, namely the ruthenium supramolecular self-assembly body containing the bipyridyl ligand. The self-assembly body is a novel ruthenium-containing self-assembly compound, and has a good inhibition effect on cancer tumor cell lines A549 and HepG-2.

Influence of heteroaryl group on electrochemical and spectroscopic properties of conjugated polymers

During our search for novel conjugated compounds, novel monomers and their polymers with selenophene and tellurophene group were synthesized and characterized. Conjugated poly(p-phenylenevinylenes)s (PPV) derivatives attracted a large attention due to their photolouminescence properties. The stereocontrolled synthesis of 1,4-bis(2-(heteroar-2-yl) ethenyl)benzenes and 1,4-bis(heteroar-2-yl)benzenes with tellurophene, selenophene, thiophene and furan-based monomers has been successfully performed. Eight of p-phenylene derivatives have been synthesized, electrochemically polymerized and characterized.