129236-97-1

Usage

Uses

Used in Detergent Industry:
1,4-Bis(decyloxy)benzene 98 is used as a surfactant and dispersant for improving the solubility and stability of detergent formulations. Its properties contribute to the effectiveness of cleaning agents by reducing the surface tension of water, allowing it to mix with oil and dirt, thus facilitating their removal from various surfaces.
Used in Emulsifier Industry:
In the emulsifier industry, 1,4-bis(decyloxy)benzene 98 is utilized as a key component in the production of emulsifiers. It aids in the formation of stable emulsions by reducing the interfacial tension between two immiscible liquids, such as oil and water, enabling them to mix and remain stable for extended periods.
Used in Organic Synthesis:
1,4-Bis(decyloxy)benzene 98 serves as an intermediate in organic synthesis, where it is used to produce a variety of other chemical compounds. Its unique structure allows for further chemical reactions, leading to the creation of new substances with different properties and applications.
Used in Materials Science:
Within the field of materials science, 1,4-bis(decyloxy)benzene 98 is employed in the development and enhancement of various materials. Its chemical properties make it a useful additive in the formulation of materials with specific characteristics, such as improved solubility, stability, or other desired attributes.

Upstream product

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• 112-29-8 1-bromo dodecane 
• 2050-77-3 Iododecane 

Downstream Products

• 152269-98-2 1,4-Dibromo-2,5-bis(decyloxy)benzene 
• 862259-95-8 [2-(2,5-bis-decyloxy-4-ethynyl-phenylethynyl)-4,5-bis-decyloxy-phenylethynyl]-triisopropyl-silane 
• 150086-27-4 1,4-diethynyl-2,5-bis(decyloxy)benzene 
• 736179-67-2 1,4-bis(decyloxy)-2-iodo-5-trimethylsilylethynylbenzene 
• 736179-69-4 1,4-bis(decyloxy)-2-ethynyl-5-triisopropylsilylethynylbenzene 
• 736179-72-9 1,4-bis(decyloxy)-2,5-bis(trimethylsilylethynyl)benzene 
• 736179-68-3 1,4-bis(decyloxy)-2-triisopropylsilylethynyl-5-trimethylsilylethynylbenzene 
• 870751-49-8 C₅₈H₉₀O₄ 
• 736179-70-7 4-[2',5'-bis(decyloxy)-4'-ethynylphenylethynyl]-2,5-bis(decyloxy)phenylethynyl-triisopropylsilane 
• 736179-60-5 C₇₀H₁₁₈O₄Si₂ 
• 942226-40-6 2-bromo-1,4-bis(decyloxy)benzene 
• 942226-41-7 (2,5-bis(decyloxy)phenyl)boronic acid 
• 1436378-07-2 2-cyanomethyl-1,4-bis(decyloxy)benzene 
• 1436378-08-3 2-bromo-5-(bromocyanomethyl)-1,4-bis(decyloxy)benzene 

Relevant academic research and scientific papers

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

Bipyridyl ligand and preparation method thereof, ruthenium supramolecular self-assembly body containing bipyridyl ligand and preparation method and application of ruthenium supramolecular self-assembly

The invention provides a novel bipyridyl bidentate ligand and a preparation method thereof. The structural formula of the novel bipyridyl bidentate ligand is shown in the specification. The inventionfurther provides a ruthenium supramolecular self-assembly body of the ligand and a preparation method of the ruthenium supramolecular self-assembly body. The preparation method comprises the followingsteps: putting a prepared ruthenium receptor and a bipyridyl ligand into a container, adding a mixed solvent of methanol and dichloromethane in equal proportion, stirring for a period of time at roomtemperature, spin-drying the solution to a certain volume after the reaction is finished, slowly adding diethyl ether, and separating out solid powder, namely the ruthenium supramolecular self-assembly body containing the bipyridyl ligand. The self-assembly body is a novel ruthenium-containing self-assembly compound, and has a good inhibition effect on cancer tumor cell lines A549 and HepG-2.

Synthesis and Properties of Triphenodioxazine-Based Conjugated Polymers for Polymer Solar Cells

As a fused-ring conjugated unit, triphenodioxazine, has been applied in two series of thiophene-free conjugated polymers for polymer solar cells. The polymers were synthesized through a multi-step synthetic route, and the substituents had a great effect on the reactivity of the reactants. Relationships among the polymer structures as well as thermal, optical, and electrochemical properties were investigated in detail by experimental data analysis and theoretical simulation. The polymers possess highly planar backbones, broad Vis/NIR absorption bands, suitable frontier molecular orbital energies, and low band gaps ranging from 1.3 to 1.8 eV. The power conversion efficiencies of their photovoltaic devices are about 1 %. Introducing longer alkyl side chains into a polymer can bring about a better film-forming ability and improve the photovoltaic performance.

Poly[(arylene ethynylene)-alt-(arylene vinylene)]s Based on Anthanthrone and Its Derivatives: Synthesis and Photophysical, Electrochemical, Electroluminescent, and Photovoltaic Properties

Anthanthrone and its derivatives are large polycyclic aromatic compounds (PACs) that pose a number of challenges for incorporation into the structure of soluble conjugated polymers. For the first time, this group of PACs was employed as the building blocks for the synthesis of copolymers (P1-P5) based on poly[(arylene ethynylene)-alt-(arylene vinylene)]s backbone (-Ph-C=C-Anth-C=C-Ph-CH - CH-Ph-CH - CH-)n. During the synthesis of P1-P5, different alkyloxy side chains were incorporated in order to tune the properties of the polymers. Of the copolymer series only P1 (containing anthanthrone and branched 2-ethylhexyloxy side chains on phenylenes), P2 and P3 (for which the anthanthrones containing carbonyl groups were converted to anthanthrene containing alkyloxy substituents) were soluble. The photophysical, electrochemical, electroluminescent and photovoltaic properties of P1-P3 are reported, compared and discussed with respect to the effects of side chains.

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.

Synthesis, spectroscopic and nonlinear optical properties of multiple [60]fullerene-oligo(p-phenylene ethynylene) hybrids

A series of multiple [60]fullerene terminated oligo(p-phenylene ethynylene) (OPE) hybrid compounds has been synthesized through a newly developed in situ ethynylation method. Structural and magnetic shielding properties of the highly unsaturated carbon-ri

Facile synthesis of multifullerene-OPE hybrids via in situ ethynylation

A series of fullerene-terminated oligo(phenylene ethynylene)s (OPEs) (1a-d and 2) have been synthesized and further characterized by cyclic voltammetry (CV) and UV-vis spectroscopy. The key step in the syntheses is an effective one-pot reaction that allow

The CA.M lattice revisited. Gel formation from a linear bis-isocyanuric acid and 2-amino-4,6-bis-(4-tert-butylphenylamino)-1,3,5-triazine

Five bis(isocyanuric) acid dimers have been prepared and characterised. The introduction of flexible alkyl chains was necessary to aid solubility. On mixing with N,N-bis(4-tert-butyphenyl)melamine in THF followed by slow evaporation, a viscous gel can form which is interpreted as evidence for the assembly of an infinite 2-D hydrogen bonded network.

Design and synthesis of metal ion-recognition-induced conjugated polymers: An approach to metal ion sensory materials

The synthesis and metal ion responsive properties of two 2,2'-bipyridyl-phenylene-vinylene-based polymers is reported. These polymers are designed to be partially conjugated in their metal-free state and fully conjugated when exposed to metal ions so that

Synthesis of Alkyl- and Alkoxy-Substituted Benzils and Oxidative Coupling to Tetraalkoxyphenanthrene-9,10-diones

Intermolecular Friedel-Crafts acylation of various substituted alkyl- or alkoxybenzenes with oxalyl chloride using carbon disulfide as solvent gave rise to the benzils 1a-k.Subsequent intramolecular oxidative coupling with either thallium(III) oxide/trifluoroacetic acid or vanadium(V) oxyfluoride/boron trifluoride diethyl etherate resulted in the corresponding phenanthrene-9,10-diones 2a-d.It has been shown that oxygen functionalities at the 3,3',4, and 4'positions are necessary for coupling to occur.These substituted benzils and phenanthrene-9,10-diones constitute precursors for ligands in the field of discotic metallomesogens or polymeric mesogens.