152269-98-2

Basic information

• Product Name: 1 4-DIBROMO-2 5-BIS(DECYLOXY)BENZENE 9&
• Synonyms: 1 4-DIBROMO-2 5-BIS(DECYLOXY)BENZENE 9&;1,4-DIBROMO-2,5-DI(DECYLOXY)BENZENE
• CAS NO: 152269-98-2
• Molecular Formula: C₂₆H₄₄Br₂O₂
• Molecular Weight: 548.43
• Product Categories: Polyphenylenevinylene (PPV, CN-PPV) Monomers;Organic Electronics and Photonics;Synthetic Tools and Reagents
• Mol File: 152269-98-2.mol
• Article Data: 7

Chemical Properties

• Melting Point: 72-76 °C(lit.)
• Boiling Point: 536.2±45.0 °C(Predicted)
• Appearance: /
• Density: 1.174±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1 4-DIBROMO-2 5-BIS(DECYLOXY)BENZENE 9&(CAS DataBase Reference)
• NIST Chemistry Reference: 1 4-DIBROMO-2 5-BIS(DECYLOXY)BENZENE 9&(152269-98-2)
• EPA Substance Registry System: 1 4-DIBROMO-2 5-BIS(DECYLOXY)BENZENE 9&(152269-98-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 152269-98-2(Hazardous Substances Data)

Usage

Uses

1,4-Dibromo-2,5-bis(decyloxy)benzene is an intermediate used in the preparation of new efficient blue light emitting polymers for light emitting diodes

Upstream product

• 129236-97-1 1,4-bis(decyloxy)benzene 
• 112-29-8 1-bromo dodecane 
• 123-31-9 hydroquinone 
• 14753-51-6 2,5-dibromohydroquinone 

Downstream Products

• 850446-24-1 2,5-didecyloxy-1,4-bis(4-formylphenyl)benzene 
• 1334177-77-3 (4-bromo-2,5-bis(decyloxy)phenyl)boronic acid 
• 1600515-41-0 1,4-bis(2',2-dithienyl)-2,5-bis(decyloxy)benzene 

Relevant articles and documents

New efficient blue light emitting polymer for light emitting diodes

The synthesis, by the Suzuki coupling reaction, of a novel soluble blue light emitting polymer, poly{(9,9-dihexyl-2,7-fluorene-alt-co-[2,5-bis(decyloxy)-1,4-phenylene]} (PDHFDDOP) is reported. PDHFDDOP exhibits photoluminescence (PL quantum efficiency of

Benzothiadiazole, hexylthiophen and alkoxy benzene based solution processable copolymer: Effect of the electron withdrawing substituents (fluorine atoms) on electrochemical, optical and electrochromic properties

4,7-Bis(4-hexyl-5-(trimethylstannane) -2-thienyl) ?2,1,3-benzothiadiazole (HTBT) coupled with 2,5-bis (decyloxy)-1,4-dibromobenzene to afford the donor-π-bridge-donor-acceptor conjugated poly (4,7-bis (4-hexyl-2-thienyl) ?2,1,3-benzothiadiazole-co-p-didec

Aryl trihydroxyborate salts: Thermally unstable species with unusual gelation abilities

A series of aryl trihydroxyborate salts were synthesized and found to form gels in benzene. The compounds were thermally unstable and readily underwent protodeboronation in solution and the solid state. Gelation could be induced without decomposition via sonication. Subsequent characterization studies revealed an unusual dependence of gel properties on alkyl chain length.