128424-36-2

Basic information

• Product Name: 1,4-DIBROMO-2,5-DI(HEXYLOXY)BENZENE
• Synonyms: 1,4-DIBROMO-2,5-DI(HEXYLOXY)BENZENE
• CAS NO: 128424-36-2
• Molecular Formula: C₁₈H₂₈Br₂O₂
• Molecular Weight: 436.22
• Mol File: 128424-36-2.mol
• Article Data: 26

Chemical Properties

• Melting Point: 51.3-53.1 °C(Solv: dichloromethane (75-09-2); methanol (67-56-1))
• Boiling Point: 436.1±40.0 °C(Predicted)
• Appearance: /
• Density: 1.302±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,4-DIBROMO-2,5-DI(HEXYLOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DIBROMO-2,5-DI(HEXYLOXY)BENZENE(128424-36-2)
• EPA Substance Registry System: 1,4-DIBROMO-2,5-DI(HEXYLOXY)BENZENE(128424-36-2)

Safety Data

• Hazardous Substances Data: 128424-36-2(Hazardous Substances Data)

Usage

General Description

1,4-Dibromo-2,5-di(hexyloxy)benzene is a chemical compound with the molecular formula C16H22Br2O2. It is a synthetic organic compound used in a variety of industrial and research applications. The compound is a member of the bromoalkoxybenzene family, which are often used as intermediates in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The hexyloxy group attached to the benzene ring provides the compound with solubility and stability in organic solvents, making it suitable for use in reaction mixtures and as a building block for more complex molecules. However, like many compounds containing bromine, 1,4-Dibromo-2,5-di(hexyloxy)benzene should be handled with care due to its potential toxicity and environmental impact.

Upstream product

• 111-25-1 1-bromo-hexane 
• 123-31-9 hydroquinone 
• 202798-00-3 2-bromo-1,4-bis(hexyloxy)benzene 
• 202798-01-4 (2,5-bis(hexyloxy)phenyl)boronic acid 
• 14753-51-6 2,5-dibromohydroquinone 
• 106-51-4 p-benzoquinone 
• 67399-93-3 1,4-dihexyloxybenzene 

Downstream Products

• 151903-52-5 1,4-bis(hexyloxy)benzene-2,5-dicarbaldehyde 
• 764710-78-3 C₃₀H₅₂B₂O₆ 
• 1220349-76-7 C₂₆H₃₃BrO₂ 
• 1618089-29-4 S,S'-(2,5-bis(hexyloxy)-1,4-phenylene) O,O,O',O'-tetraisopropyldiphosphorothioate 
• 1618089-30-7 tetraisopropyl (2,5-bis(hexyloxy)-3,6-dimercapto-1,4-phenylene)bisphosphonate 
• 1618089-31-8 3,6-bis(hexyloxy)-1,4-dimercapto-2,5-diphosphinobenzene 
• 1618089-32-9 4,8-bis(hexyloxy)-2,6-diphenylbenzo[1,2-d:4,5-d']bis([1,3]thiaphosphole) 
• 1618089-35-2 4,8-bis(hexyloxy)-2,6-bis(4-methoxyphenyl)benzo[1,2-d:4,5-d']bis([1,3]thiaphosphole) 
• 1618089-36-3 4,4'-(4,8-bis(hexyloxy)benzo[1,2-d:4,5-d']bis([1,3]thiaphosphole)-2,6-diyl)dibenzonitrile 
• 1618089-28-3 2,5-bis(hexyloxy)benzene-1,4-dithiol 
• 496965-02-7 2,5-dihexyloxybenzene-1,4-dicarbonitrile 
• 1228971-03-6 4,4'-((2,5-bis(hexyloxy)-1,4-phenylene)bis(ethyne-2,1-diyl))dibenzoate 

Relevant articles and documents

Synthesis and characterization of a new conjugated polymer containing cyano substituents for light-emitting diodes

A new luminescent conjugated polymer (CN-P3PV) containing cyano groups as electron transporting units was synthesized by a Suzuki coupling reaction. CN-P3PV was characterized by 1H NMR, FT-IR, GPC, DSC, and TGA. The synthesized polymer possessed high thermal stability (Td = 360 °C, Tg= 151 °C), high electron affinity, and good thin-film forming ability. Electrical characterization of a double-layer organic LED based on the structure of ITO/CuPc/CN-P3PV/Ca/Ag showed high electron transporting ability and good electroluminescence performance with the emission of bright orange light.

Dyes for sensitized solar cells by using [2.2]paracyclophane as a bridging unit

Organic dyes that consist of a [2.2]paracyclophane moiety between a triphenylamine donor group and a cyanoacrylic acid acceptor group have exhibited considerably high values of open-circuit voltage (Voc) in the range of 0.69-0.74 V. In an exper

Synthesis and characterization of 2,2′-bithiophene end-capped dihexyloxy phenylene pentamer and its application in a solution-processed organic ultraviolet photodetector

In this work a new solution processable small organic material, namely 2,2′-bithiophene end-capped dihexyloxy phenylene pentamer (BHBT2) was synthesized, characterized and applied in the fabrication of an organic ultraviolet photodetector. The

Syntheses and emission properties of novel violet-blue emissive aromatic bis(diazaborole)s

Violet-blue emission from novel aromatic bis(diazaborole)s, which were synthesized by the reaction of 2,5-bis(hexyloxy)-1,4-phenylenediboronic acid and 1,2-phenylenediamine derivatives or diaminonaphthalene derivatives, is described. White-blue emission front a 4-methoxy-1,2-phenylenediamine-derived molecule was observed in DMF using 340 nm as the excitation wavelength.

A study on the synthesis, characterization, structural optimization, and conformational behaviors of bromo-substituted pyromelliticdiimide-based [2+2] macrocycle as structural units of covalently linked molecular tubes

Synthesis and structural, photo physical, and conformational behaviors at variable temperature and structural optimization of the pyromelliticdiimide-based bromo-substituted [2 + 2] macrocycles are described. Cyclization of the diamine (3) with dianhydride (4) in THF, followed by dehydration of the resultant amic acids resulted in the isolation of the bromo-substituted [2 + 2] macrocycle 1 (4.5%). The dynamic temperature-dependent 1H NMR spectra and MO calculations revealed the presence of two possible conformers for the [2 + 2] macrocycle 1. The UV/Vis spectrum of 1 reveals the presence of a weak intramolecular CT interaction of electron-withdrawing pyromelliticdiimide moiety with the electron-donating hexyloxy-substituted xylyl moiety. The cyclic voltammetric measurement shows two two-electron reversible reduction processes.