122996-59-2

Basic information

• Product Name: Benzene, 1,4-bis(bromomethyl)-2,5-bis(dodecyloxy)-
• CAS NO: 122996-59-2
• Molecular Formula: C32H56Br2O2
• Molecular Weight: 632.603
• Mol File: 122996-59-2.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzene, 1,4-bis(bromomethyl)-2,5-bis(dodecyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,4-bis(bromomethyl)-2,5-bis(dodecyloxy)-(122996-59-2)
• EPA Substance Registry System: Benzene, 1,4-bis(bromomethyl)-2,5-bis(dodecyloxy)-(122996-59-2)

Safety Data

• Hazardous Substances Data: 122996-59-2(Hazardous Substances Data)

Upstream product

• 123-31-9 hydroquinone 
• 143-15-7 1-dodecylbromide 
• 50-00-0 formaldehyd 
• 3230-09-9 1,4-bis-dodecyloxy-benzene 

Downstream Products

• 237757-95-8 2,5-bis(acetyl methyl)-1,4-bis(dodecyloxy)benzene 
• 737581-58-7 1,4-bis(cyanomethyl)-2,5-bis(dodecyloxy)benzene 
• 1374792-37-6 C₈₀H₁₀₈N₆O₂ 
• 1333388-09-2 C₅₄H₆₆N₄O₂ 
• 1070789-18-2 2,5-bis(dodecyloxy)-1,4-bis[2-(4-formylphenyl)ethenyl]benzene 
• 237757-97-0 2,5-bis(hydroxymethyl)-1,4-bis(dodecyloxy)benzene 
• 123415-45-2 1,4-di(n-dodecyloxy)benzene-2,5-dicarboxaldehyde 

Relevant articles and documents

Influence from thermal elimination temperature of precursor polymer and film-forming methods on the photophysics of the poly(2,5-didodecyloxy-p- phenylenevinylene)

A series of poly(p-phenylenevinylene)s (PPVs) with good solubility were synthesized from thermal elimination of precursor poly(2,5-didodecyloxy-p- phenylenevinylene) at different temperature via Wessling method. The polymer photophysics were influenced by

Isothermal and non-isothermal cold crystallization of tetrabenzofluorene (TBF) molecules

Design and synthesis of tetrabenzo[a,c,g,i]fluorene (TBF) derivatives are carried out to investigate the isothermal and non-isothermal cold crystallization (CC) behavior by various spectroscopic and analytical techniques. The unprecedented CC exhibited by

Electron donating group stimulated aggregation induced emission enhancement of oligophenylenevinylene-cored luminogens

Three new oligophenylenevinylene (OligoPV)-cored luminogens were synthesized by utilizing the Suzuki coupling/Buchwald-Hartwig amination reaction and their aggregation-induced emission properties have been studied. Out of three, two are aggregation-induce

Synthesis and spectral characterization of photoswitchable oligo(p-phenylenevinylene)-spiropyran dyad

In view of designing a new class of photoswitchable fluorescence probes and operating them in solution as well as on solid substrates, we have envisioned the possibility of attaching photochromic spiropyran (SP) to the highly efficient fluorophore oligo(p

Hexaphenylbenzene end-capped tri(p-phenylenevinylenes): Synthesis and properties

Three new hexaphenylbenzene end-capped tri(p-phenylenevinylenes) were synthesized by the Horner-Wadsworth-Emmons reaction in good yields (86-76%). All compounds have bright fluorescent emissions in the blue to blue-green region in solution (λmax/sub

Fluorescent cross-linked supramolecular polymers constructed from a novel self-complementary AABB-type heteromultitopic monomer

A novel AABB-type heteromultitopic monomer (APOPV), having a self-complementary perpendicular structure, could solely self-assemble to fluorescent cross-linked supramolecular polymers. Interestingly, the supramolecular gel film shows a sensitive fluoresce