4371-32-8

Basic information

• Product Name: [1,1-Biphenyl]-2,2,5,5-tetrol(9CI)
• Synonyms: [1,1-Biphenyl]-2,2,5,5-tetrol(9CI)
• CAS NO: 4371-32-8
• Molecular Formula: C₁₂H₁₀O₄
• Molecular Weight: 0
• Product Categories: BIPHENYL
• Mol File: 4371-32-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [1,1-Biphenyl]-2,2,5,5-tetrol(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1-Biphenyl]-2,2,5,5-tetrol(9CI)(4371-32-8)
• EPA Substance Registry System: [1,1-Biphenyl]-2,2,5,5-tetrol(9CI)(4371-32-8)

Safety Data

• Hazardous Substances Data: 4371-32-8(Hazardous Substances Data)

Usage

Description

[1,1-Biphenyl]-2,2,5,5-tetrol(9CI), also known as 2,2',5,5'-Tetrahydroxy[1,1'-biphenyl]-4,4'-dicarbinol, is a chemical compound with the molecular formula C12H12O4. It is a tetrol consisting of a biphenyl unit with hydroxy substituents at the 2, 2', 5, and 5' positions. [1,1-Biphenyl]-2,2,5,5-tetrol(9CI) is not widely studied, and there is limited information available about its properties and potential uses. However, it is likely to have applications in organic synthesis and as a building block in the development of new compounds for pharmaceutical or materials science research. Further research is needed to fully understand the potential applications and properties of [1,1-Biphenyl]-2,2,5,5-tetrol(9CI).

Uses

Used in Organic Synthesis:
[1,1-Biphenyl]-2,2,5,5-tetrol(9CI) is used as a building block in organic synthesis for the development of new compounds. Its unique structure with hydroxy substituents at specific positions allows for further chemical modifications and the creation of a variety of complex molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [1,1-Biphenyl]-2,2,5,5-tetrol(9CI) is used as a starting material for the development of new drugs. Its structural features make it a promising candidate for the synthesis of bioactive molecules with potential therapeutic applications.
Used in Materials Science Research:
[1,1-Biphenyl]-2,2,5,5-tetrol(9CI) is also used in materials science research to explore its potential as a component in the development of new materials with specific properties, such as improved stability, reactivity, or biocompatibility.

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Relevant articles and documents

Electrochemically manipulating the redox state of 2,2′,5,5′-tetrahydroxybiphenyl as a new organic Li-rich cathode for Li-ion batteries

For the first time, a small organic molecule of 2,2′,5,5′-tetrahydroxybiphenyl (BP4OH) is synthesized as a new organic cathode for Li-ion batteries. After setting reduction in the 1st cycle in Li-ion half cells (reduction→oxidation), BP4OH can be in-situ transformed to its salt of lithium 2,2′-bis[benzene-1,4-bis(olate)] (BP4OLi) on Al foil. The resulting BP4OLi is a Li-rich organic cathode and exhibits very good cell performance. For example, the average capacity of ~155 mAh g?1 for the BP4OLi electrode is realized during 600 cycles (500 mA g?1). On the other hand, after setting oxidation in the 1st cycle (oxidation→reduction), BP4OH can be in-situ tuned to its oxidized state of 2,2′-bis(1,4-benzoquinone) (BBQ). Interestingly, the resulting BBQ can be still redox-active and show satisfactory cell performance. For instance, the average capacity of ~101 mAh g?1 for the BBQ electrode can be obtained for 600 cycles (500 mA g?1). This work reveals very interesting redox behaviors of organic electrodes.

p-Doped high spin polymers

High spin polymers have been created from p-doping of networked polyaryl and polyarylamine polymers which were synthesized using the Pd0 mediated coupling reaction of aryl di- and tri-bromides with aryl bis- and tris-boronic acids. The doping p

Regiochemical Control in the Oxidative Coupling of Metal Phenolates: Highly Selective Synthesis of Symmetric, Hydroxylated Biaryls

Oxidative coupling of highly coordinating metal phenolates promoted by FeCl3 afforded variously substituted symmetric 2,2'-dihydroxy biaryls in good yield and high regiochemical control. Key words: Oxidative coupling; metal phenolates; 2,2'-dihydroxy biar