15764-52-0

Usage

Uses

Used in Polymer Production:
2,2'-DIHYDROXYDIPHENYL ETHER serves as a crucial chemical intermediate in the synthesis of a range of polymers. Its primary applications are observed in the manufacturing processes of epoxy resins and polyesters, where it contributes to the formation of polymers with enhanced properties.
Used in Rubber and Lubricant Industries:
As an antioxidant, 2,2'-DIHYDROXYDIPHENYL ETHER is integrated into rubbers and lubricants to extend their service life by preventing oxidative degradation. This function is vital for maintaining the performance and reliability of these materials in various applications.
Used in Plastics Industry:
In the plastics industry, particularly with PVC, 2,2'-DIHYDROXYDIPHENYL ETHER operates as a stabilizer. It helps to prevent the degradation of PVC under heat and light exposure, thereby preserving the plastic's structural integrity and performance.
Used in Flame Retardancy:
2,2'-DIHYDROXYDIPHENYL ETHER has been explored for its potential as a flame retardant. Its incorporation into materials can potentially enhance their fire resistance, making it a valuable component in industries where flame retardancy is a critical safety requirement.
Used in Metal Extraction:
Furthermore, 2,2'-DIHYDROXYDIPHENYL ETHER has been considered for its chelating properties in metal extraction processes. It can bind to metal ions, facilitating their separation and recovery from various sources.
Environmental Considerations:
Given the limited information on the toxicity and environmental impact of 2,2'-DIHYDROXYDIPHENYL ETHER, it is imperative to adhere to proper handling and disposal procedures to mitigate any potential risks to human health and the environment.

Upstream product

• 32503-27-8 tetra(n-butyl)ammonium hydrogensulfate 
• 584-08-7 potassium carbonate 
• 120-80-9 benzene-1,2-diol 
• 95-56-7 2-hydroxybromobenzene 
• 67274-34-4 trimethyl(9H-xanthen-9-yl)silane 
• 92-83-1 xanthene 
• 101-84-8 diphenylether 
• 121-43-7 Trimethyl borate 
• 1655-70-5 di(2-methoxyphenyl) ether 

Downstream Products

• 262-12-4 dioxin 
• 22649-30-5 2,2'-dihydroxy-5,5'-dibromodiphenyl ether 
• 22649-31-6 6,6′-dihydroxy-2,2′,4,4′-tetrabromodiphenyl ether 
• 96476-01-6 Oxybis(2,1-phenylenoxy-N,N-dicyclohexylacetamid) 
• 86045-00-3 2,2'-diphenol-dibenzylether 
• 72011-23-5 dibenzo-15-crown-5-ether 
• 311344-41-9 2-(2-tetrahydropyranyloxyphenoxy)phenol 
• 1352312-27-6 [(phenyl)Al(2,2'-oxobis(phenolato))]2 
• 120-80-9 benzene-1,2-diol 
• 108-95-2 phenol 

Relevant academic research and scientific papers

Catalytic Double Carbon–Boron Bond Formation for the Synthesis of Cyclic Diarylborinic Acids as Versatile Building Blocks for π-Extended Heteroarenes

The first catalytic synthesis of cyclic diarylborinic acids is developed using a dihydroaminoborane reagent as the boron source. Unlike previously reported methods that use organolithium reagents, this method allows the easy synthesis of cyclic diarylbori

Structural Elucidation of Selective Solvatochromism in a Responsive-at-Metal Cyclometalated Platinum(II) Complex

We report the synthesis, characterization, and spectroscopic investigations of a new responsive-at-metal cyclometalated platinum(II) complex. With mild chemical oxidants and reductants, it was possible to obtain the same complex in three different oxidati

Multiresponsive Cyclometalated Crown Ether Bearing a Platinum(II) Metal Center

Multiresponsive materials can adapt to numerous changes in their local environment, which makes them highly valuable for various applications. Although nanostructured and polymeric multiresponsive materials are plentiful, small-molecule analogues are scarce. This work presents a compact cyclometalated platinum(II) complex that bears a crown ether cavity (18C6-PtII); the intimate ring/emitter connectivity is key to unlocking multiresponsiveness. Complex 18C6-PtII responds to (i) cationic guests, producing changes in luminescence in both solution and the solid state, (ii) solvent molecules, which perturb the packing of the complex in the solid state and cause reversible color changes, and (iii) solvent polarity, which leads to controlled aggregation. These responses may enable 18C6-PtII to function as a sensor for ions and solvents, or as a functional unit for the fabrication of hybrid supramolecular polymers and metallogels.

Synthesis technology of o-hydroxy phenyl ethyl ether

The invention discloses a synthesis technology of o-hydroxy phenyl ethyl ether. The synthesis technology takes catechol as a raw material, diethyl carbonate as an alkylating reagent, and titanium-zirconium load type phosphoric acid as a catalyst; a prepar

Direct oxidation of the C(sp2)-C(sp3) bond from benzyltrimethylsilanes to phenols

A novel pathway for direct conversion of benzylsilanes to phenols by oxidation with Na2S2O8 and oxygen is efficiently developed under mild and neutral conditions. The reaction shows good functional group tolerance to afford phenols in moderate yields. The possible mechanism is proposed based on the isotopic labeling trials.

Synthesis, Ion Recognition Ability, and Metal-Assisted Aggregation Behavior of Dinuclear Metallohosts Having a Bis(Saloph) Macrocyclic Ligand

Macrocyclic molecule 1 that has two saloph coordination sites was designed and synthesized. The macrocycle 1 was easily converted into the corresponding metallohosts 2 and 3 by the reaction with nickel(II) and palladium(II), respectively. As expected from

Copper(II)-catalyzed hydroxylation of aryl halides using glycolic acid as a ligand

Copper(II)-catalyzed hydroxylation of aryl halides has been developed to afford functionalized phenols. The protocol utilizes the reagent combination of Cu(OH)2, glycolic acid, and NaOH in aqueous DMSO, all of which are cheap, readily available, and easily removable after the reaction. A broad range of aryl iodides and activated aryl bromides were transformed into the corresponding phenols in excellent yields. Moreover, it has been shown that C-O(alkyl)-coupled product, instead of phenol, can be predominantly formed under similar reaction conditions.

Highly efficient regulation of cation recognition and promotion of self-assembly by metalation of a macrocyclic bis(N2O2) ligand with nickel(ii)

Metalation of a bis(N2O2) macrocyclic ligand 1 with nickel(ii) acetate afforded a dinuclear metallohost 2, resulting in a significant enhancement of recognition ability of alkali metal ions and the promotion of self-aggregation.

Process for the stereoselective preparation of a hetero-bicyclic alcohol enantiomer

The invention relates to a method for the stereoselective preparation of a hetero-bicyclic alcohol enantiomer, characterized in that a substantially pure enantiomer of the general formula STR1 is prepared from a compound of the general formula STR2 wherein the variable are as defined as in claim 1. The method comprises the following successive reaction steps: (i) reaction with a substantially enantiomerically pure compound of the general formula STR3 wherein Z, R3 and R4 are defined as in claim 1; (ii) subjection of the compound formed to a deprotection/ring-closure reaction; (iii) optionally deprotection of the hydroxy group of the ring-closed product. The invention further relates to enantiomerically pure intermediates, the preparation of these intermediates and the preparation of a starting compound.

Macroring-Neutral Molecule Complexation. Synthesis of Biconcave Pyridino Hosts, Complex Formation, and X-ray Crystal Structures of Two Inclusion Compounds

A series of pyridino macrocycles 1-3(a-e) incorporating rigid bi- and triaryl ether segments in different ring positions have been synthesized.The effect of incorporation of these building blocks into a given macroring framework on the host properties for