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

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

Downstream Products

• 564456-59-3 2,5-bis(butoxy)benzene-1,4-dialdehyde 
• 1262137-07-4 4-bromo-2,5-bis(butoxy)benzaldehyde 
• 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 
• 380626-51-7 1,4-dibutoxy-2,5-bis(thiophen-2-yl)benzene 
• 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 
• 380626-58-4 1,4-dibutoxy-2,5-di(5'-phenyl-5''-di-2',2''-thienyl)benzene 
• 380626-53-9 1,4-di-n-butoxy-2,5-di(2'-iodo-5'-thienyl)benzene 
• 128834-29-7 1,4-bis(ethynyl)-2,5-di(butyloxy)benzene 
• 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 

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.

Boronate Ester-Capped Helicates

Triple-stranded helicates were obtained by metal-templated multicomponent reactions of bispyridyloxime ligands with arylboronic acids. The helicates feature two hexa-coordinated MII ions (M=Fe, Zn, or Mn), which are embedded in a macrobicyclic ligand framework, and two arylboronate ester capping groups. The latter can be used to introduce functional groups such as pyridines, aldehydes, nitriles, and carboxylic acids in apical position. The functionalized helicates have the potential to be used as nanoscale building blocks for more complex assemblies, as evidenced by the synthesis of a 3 nm-sized trianglimine.

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.