233661-07-9

Basic information

• Product Name: 1-bromo-3,4-bis(decyloxy)benzene
• Synonyms: 1-bromo-3,4-bis(decyloxy)benzene
• CAS NO: 233661-07-9
• Molecular Weight: 469.546
• Mol File: 233661-07-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-bromo-3,4-bis(decyloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-3,4-bis(decyloxy)benzene(233661-07-9)
• EPA Substance Registry System: 1-bromo-3,4-bis(decyloxy)benzene(233661-07-9)

Safety Data

• Hazardous Substances Data: 233661-07-9(Hazardous Substances Data)

Upstream product

• 112-29-8 1-bromo dodecane 
• 16492-75-4 5-bromo-1,2,3 trihydroxybenzene 
• 2859-78-1 4-Bromoveratrole 
• 17345-77-6 1-bromo-3,4-dihydroxybenzene 
• 25934-47-8 1,2-bis-decyloxy-benzene 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 233661-05-7 (3,4-bis(decyloxy)phenyl)boronic acid 
• 881209-82-1 2-[3,4-bis(decyloxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant articles and documents

Smectic and columnar liquid crystalline phases through charge-transfer interactions

New heterocyclic electron donors based on a 1,3,5-triazine nucleus are presented. Three phenyl rings are grafted to the triazine core either via secondary amino groups or by a direct C,C-linkage and a specific number of decyloxy chains is attached to the

Molecular design of benzothienobenzothiophene-cored columnar mesogens: Facile synthesis, mesomorphism, and charge carrier mobility

Benzothienobenzothiophene (BTBT) liquid-crystalline semiconductors are arousing a lot of interest due to their long-range ordered, self-organizational abilities and high-charge carrier transport properties. In this work, we report the design and the straightforward synthesis of a homologous series of compounds containing the BTBT substructure by the successive Suzuki cross-coupling and FeCl3 oxidative Scholl cyclodehydrogenation reaction. Target π-conjugated aromatic, H-shaped sanidic mesogens self-organize into a classical hexagonal columnar mesophase over wide temperature ranges as deduced from polarized optical microscopy (POM), differential scanning calorimetry (DSC), and small-angle X-ray scattering (SAXS) investigations. UV/Vis absorption and photoluminescence spectra, measured in both solution and films, revealed strong photoluminescence with high quantum yields. The charge carrier mobility measured by the time-of-flight (TOF) technique showed a balanced ambipolar hole and electron mobility in the range of 10-3 cm2 V-1 s-1 between 100 and 230 °C in the mesophase. These BTBT-based columnar liquid crystals may represent attractive candidates to be incorporated within one-dimensional organic optoelectronic devices.

Thermotropic properties and molecular packing of discotic tristriazolotriazines with rigid substituents

Tristriazolotriazines with a threefold dialkoxyaryl substitution have been prepared by Huisgen reaction of cyanuric chloride and the corresponding tetrazoles. Although these dyes show a negative or inverted solvatochromism of the UV/Vis absorption, their

Columnar and smectic liquid crystals based on crown ethers

Unsymmetrical benzo[15]-crown-5 ethers 5 with one lateral ortho-terphenyl unit bearing alkoxy side chains of varying chain lengths (C5-C14) were prepared from 3,4-dialkoxyphenylbromides 2. Complexation with metal salts MX (M = Na, Cs) afforded the corresp