15764-52-0

Basic information

• Product Name: 2,2'-DIHYDROXYDIPHENYL ETHER
• Synonyms: 2,2'-OXYDIPHENOL;2,2'-OXYBISPHENOL;2,2'-DIHYDROXYDIPHENYL ETHER;2-HYDROXYPHENYL ETHER;BIS(2-HYDROXYPHENYL) ETHER;2,2''-DIHYDROXYDIPHENYL ETHER 98+%;Bis(2-hydroxyphenyl) Ether 2-Hydroxyphenyl Ether 2,2'-Oxybisphenol 2,2'-Oxydiphenol
• CAS NO: 15764-52-0
• Molecular Formula: C₁₂H₁₀O₃
• Molecular Weight: 202.21
• Product Categories: Diphenyl Ethers (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer Research
• Mol File: 15764-52-0.mol
• Article Data: 12

Chemical Properties

• Melting Point: 123°C
• Boiling Point: 299.3°Cat760mmHg
• Flash Point: 134.8°C
• Appearance: /
• Density: 1.288g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: very faint turbidity in Methanol
• CAS DataBase Reference: 2,2'-DIHYDROXYDIPHENYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-DIHYDROXYDIPHENYL ETHER(15764-52-0)
• EPA Substance Registry System: 2,2'-DIHYDROXYDIPHENYL ETHER(15764-52-0)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 15764-52-0(Hazardous Substances Data)

Usage

General Description

2,2'-DIHYDROXYDIPHENYL ETHER, also known as 2,2’-dihydroxybiphenyl or 2,2’-biphenol, is an organic compound with the chemical formula C12H10O2. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. 2,2'-DIHYDROXYDIPHENYL ETHER is used as a chemical intermediate in the production of various polymers, particularly in the manufacturing of epoxy resins and polyesters. It is also utilized as an antioxidant in rubbers and lubricants, as well as a stabilizer in PVC plastics. Additionally, it has been investigated for its potential as a flame retardant and as a chelating agent in metal extraction processes. However, there is limited information available on its toxicity and environmental impact, so proper handling and disposal procedures should be followed.

Upstream product

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

Downstream Products

• 473827-99-5 5,22-Dibromo-2,9,12,15,18-pentaoxa-tricyclo[17.4.0.0^3,8]tricosa-1⁽²³⁾,3⁽⁸⁾,4,6,19,21-hexaene 
• 72011-23-5 dibenzo-15-crown-5-ether 
• 262-12-4 dioxin 
• 311344-41-9 2-(2-tetrahydropyranyloxyphenoxy)phenol 
• 120-80-9 benzene-1,2-diol 
• 108-95-2 phenol 
• 1352312-27-6 [(phenyl)Al(2,2'-oxobis(phenolato))]2 
• 86045-03-6 2,2'-diphenol 
• 311344-42-0 1,2,4,5-tetrakis[2-(2-tetrahydropyranyloxyphenoxy)phenoxymethyl]benzene 
• 311344-43-1 1,2,4,5-tetrakis[2-(2-hydroxyphenoxy)phenoxymethyl]benzene 

Relevant articles and documents

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

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.