137436-30-7

Basic information

• Product Name: 1,4-DIBROMO-2,5-DI(DODECYLOXY)BENZENE
• Synonyms: 1,4-DIBROMO-2,5-DI(DODECYLOXY)BENZENE;1,4-didodecyloxy-2,5-dibromobenzene
• CAS NO: 137436-30-7
• Molecular Formula: C₃₀H₅₂Br₂O₂
• Molecular Weight: 604.54
• Mol File: 137436-30-7.mol
• Article Data: 14

Chemical Properties

• Melting Point: 77-78 °C
• Boiling Point: 581.8±45.0 °C(Predicted)
• Appearance: /
• Density: 1.134±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,4-DIBROMO-2,5-DI(DODECYLOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DIBROMO-2,5-DI(DODECYLOXY)BENZENE(137436-30-7)
• EPA Substance Registry System: 1,4-DIBROMO-2,5-DI(DODECYLOXY)BENZENE(137436-30-7)

Safety Data

• Hazardous Substances Data: 137436-30-7(Hazardous Substances Data)

Usage

General Description

1,4-DIBROMO-2,5-DI(DODECYLOXY)BENZENE is a compound with the chemical formula C30H48Br2O2. It is a derivative of benzene and contains two bromine atoms and two dodecyloxy (C12H25O) groups attached to the benzene ring. This chemical is commonly used in the production of surfactants, which are compounds that reduce the surface tension between two liquids or between a liquid and a solid. Surfactants have a wide range of industrial applications, including use in detergents, emulsifiers, and foaming agents. The presence of bromine atoms in 1,4-DIBROMO-2,5-DI(DODECYLOXY)BENZENE makes it useful in flame retardant formulations and other fire-resistant materials. Additionally, the dodecyloxy groups contribute to the compound's surfactant properties, making it an effective and versatile chemical in various industrial processes.

Upstream product

• 3230-09-9 1,4-bis-dodecyloxy-benzene 
• 14753-51-6 2,5-dibromohydroquinone 
• 143-15-7 1-dodecylbromide 
• 123-31-9 hydroquinone 

Downstream Products

• 1311149-61-7 C₅₂H₇₄O₈ 
• 364336-10-7 2,5-dibromo-4-dodecyloxyphenol 
• 152270-19-4 ((2,5-bis(dodecyloxy)-1,4-phenylene)bis(ethyne-2,1-diyl))bis(trimethylsilane) 
• 264282-37-3 5-(4-bromo-2,5-bis(dodecyloxy)phenyl)-2,3-dihydrothieno[3,4-b][1,4]dioxine 
• 1008132-03-3 2-(4-bromo-2,5-bis(dodecyloxy)phenyl)thiophene 
• 277316-25-3 1-(3-hydroxy-3-methyl-1-butynyl)-2,5-di(dodecyloxy)-4-[(2,6-bis(2-pyridinyl)pyridine-4-yl)ethynyl]benzene 
• 243835-44-1 1-[(4-bromo-2,5-di(dodecyloxy)phenyl)ethynyl]-2,5-di(dodecyloxy)-4-[(2,6-bis(2-pyridinyl)pyridine-4-yl)ethynyl]benzene 
• 243835-42-9 1-ethynyl-2,5-di(dodecyloxy)-4-[(2,6-bis(2-pyridinyl)pyridine-4-yl)ethynyl]benzene 
• 243835-38-3 1-(3-hydroxy-3-methyl-1-butynyl)-4-ethynyl-2,5-di(dodecyloxy)benzene 
• 152270-00-3 1,4-bis(dodecyloxy)-2,5-diethynylbenzene 
• 874115-28-3 C₈₇H₁₃₁N₃O₄Si 
• 874115-27-2 C₈₂H₁₂₂BrN₃O₄ 

Relevant articles and documents

Synthesis and characterization of thiophene and thieno[3,2-b]thiophene containing conjugated polymers

Herein, we report the synthesis of two donor-acceptor-donor polymers (P1 and P2) based on thiophene (M1) and thieno [3,2-b]thiophene (M2) as the donor and 2,5-bis(dodecyloxy)benzene as the acceptor unit. The effects of different donor units on the polymer

Hierarchical self-assembly of p-terphenyl derivative with dumbbell-like amphiphilic and rod-coil characteristics

As water is gradually added, a p-terphenyl derivative with dumbbell-like amphiphilic and rod-coil characteristics can hierarchically self-assemble to metastable rectangle columns architecting sheets first and then to stable quasi-hexagonal columns architecting rolled sheets, and finally to rod-like nanostructures in MeOH/H2O solution. Interestingly, the formed sheet, rolled sheet, and nanorod possess blue-light emitting property.

Eumelanin-inspired core derived from vanillin: A new building block for organic semiconductors

An eumelanin-inspired core derived from the natural product, vanillin (vanilla bean extract) was utilized for the synthesis of eumelanin-inspired small molecules and polymer via Sonogashira cross coupling. The materials demonstrate that the methyl 4,7-dibromo-5,6-dimethoxy-N-methyl-1H-indole-2-carboxylate core can serve as a new building block for organic semiconductors.

Supramolecular ruthenium-alkynyl multicomponent architectures: Engineering, photophysical properties, and responsiveness to nitroaromatics

A series of H-bonded supramolecular architectures were built from monofunctional M-Ci - C-R and bifunctional R-Ci - C-M-Ci - C-R trans-alkynylbis(1,2-bis(diphenylphosphino)ethane)ruthenium(II) complexes and π-conjugated modules containing 2,5-dialkoxy-p-p