145483-68-7

Basic information

• Product Name: 1,4-DIIODO-2,5-BIS(OCTYLOXY)BENZENE
• Synonyms: 1,4-DIIODO-2,5-BIS(OCTYLOXY)BENZENE;Benzene, 1,4-diiodo-2,5-bis(octyloxy)-
• CAS NO: 145483-68-7
• Molecular Formula: C₂₂H₃₆I₂O₂
• Molecular Weight: 586.33
• Mol File: 145483-68-7.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-DIIODO-2,5-BIS(OCTYLOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DIIODO-2,5-BIS(OCTYLOXY)BENZENE(145483-68-7)
• EPA Substance Registry System: 1,4-DIIODO-2,5-BIS(OCTYLOXY)BENZENE(145483-68-7)

Safety Data

• Hazardous Substances Data: 145483-68-7(Hazardous Substances Data)

Usage

Description

1,4-Diiodo-2,5-bis(octyloxy)benzene is an organic compound characterized by its molecular structure that features a benzene ring with two iodine atoms at the 1,4 positions and two octyloxy groups at the 2,5 positions. 1,4-DIIODO-2,5-BIS(OCTYLOXY)BENZENE is known for its unique properties and potential applications in various fields.

Uses

1. Used in Polymer Synthesis:
1,4-Diiodo-2,5-bis(octyloxy)benzene is used as an intermediate in the synthesis of hybrid block copolymers. The compound plays a crucial role in the formation of these copolymers, which are composed of conjugated poly(phenyleneethylene) (PPE) and stereoregular poly(Ph isocyanide) (PPI) segments. The use of a palladium(II) complex as a single catalyst in the synthesis process allows for the efficient and controlled formation of these hybrid copolymers.
2. Used in the Chemical Industry:
In the chemical industry, 1,4-diiodo-2,5-bis(octyloxy)benzene can be utilized as a building block for the development of new materials with specific properties. Its unique structure and functional groups make it a valuable component in the synthesis of various compounds, including those with potential applications in electronics, pharmaceuticals, and other advanced technologies.
3. Used in Research and Development:
Due to its unique structure and properties, 1,4-diiodo-2,5-bis(octyloxy)benzene is also used in research and development for exploring new chemical reactions, mechanisms, and applications. Scientists and researchers can leverage this compound to study its reactivity, stability, and potential interactions with other molecules, leading to the discovery of new chemical processes and materials.

Upstream product

• 67399-94-4 1,4-bis(octyloxy)benzene 
• 111-83-1 1-bromo-octane 
• 123-31-9 hydroquinone 
• 629-27-6 1-Iodooctane 
• 51560-21-5 1,4-diiodo-2,5-dimethoxybenzene 
• 13064-64-7 2,5-diiodo-1,4-hydroquinone 
• 150-78-7 1,4-dimethoxybezene 

Downstream Products

• 153033-27-3 1,4-diethynyl-2,5-bis(octoxy)benzene 
• 347307-94-2 1,4-bis(octyloxy)-2,5-bis(1-trimethyl-silylethenyl)benzene 
• 7342-47-4 tributyltin iodide 
• 173428-81-4 1,4-bis[(trimethylsilyl)-ethynyl]-2,5-bis-(octoxy)benzene 
• 123440-34-6 2,5-bis(octyloxy)-1,4-benzenecarboxaldehyde 
• 916081-51-1 4,4'-(2,5-bis(octyloxy)-1,4-phenylene)bis(ethyne-2,1-diyl)dibenzonitrile 
• 916081-52-2 4,4'-(4,4'-(2,5-bis(octyloxy)-1,4-phenylene)bis(ethyne-2,1-diyl)bis(4,1-phenylene))bis(ethyne-2,1-diyl)dibenzonitrile 
• 350230-73-8 2,5-bis(octyloxy)-4-[(triisopropylsilyl)ethynyl]benzaldehyde 
• 350230-75-0 {[4-ethynyl-2,5-bis(octyloxy)phenyl]ethynyl}triisopropylsilane 
• 350230-74-9 {[4-(2,2-dibromoethenyl)-2,5-bis(octyloxy)phenyl]ethynyl}triisopropylsilane 
• 350230-76-1 4-{{2,5-bis(octyloxy)-4-[(triisopropylsilyl)ethynyl]phenyl}ethynyl}-2,5-bis(octyloxy)benzaldehyde 
• 350230-77-2 {{4-{[4-ethynyl-2,5-bis(octyloxy)phenyl]ethynyl}-2,5-bis(octyloxy)phenyl}ethynyl}triisopropylsilane 
• 839683-71-5 {{4-{[4-(2,2-dibromoethenyl)-2,5-bis(octyloxy)phenyl]ethynyl}-2,5-bis(octyloxy)phenyl}ethynyl}triisopropylsilane 
• 350230-78-3 4-{{4-{{2,5-bis(octyloxy)-4-[(triisopropylsilyl)ethynyl]phenyl}ethynyl}-2,5-bis(octyloxy)phenyl}ethynyl}-2,5-bis(ocyloxy)benzaldehyde 

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