3598-29-6

Basic information

• Product Name: [1,1-Biphenyl]-3,4,4-triol (9CI)
• Synonyms: [1,1-Biphenyl]-3,4,4-triol (9CI)
• CAS NO: 3598-29-6
• Molecular Formula: C12H11O3
• Molecular Weight: 203.21394
• Product Categories: ALCOHOL
• Mol File: 3598-29-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 416.5°Cat760mmHg
• Flash Point: 210°C
• Appearance: /
• Density: 1.347g/cm³
• CAS DataBase Reference: [1,1-Biphenyl]-3,4,4-triol (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1-Biphenyl]-3,4,4-triol (9CI)(3598-29-6)
• EPA Substance Registry System: [1,1-Biphenyl]-3,4,4-triol (9CI)(3598-29-6)

Safety Data

• Hazardous Substances Data: 3598-29-6(Hazardous Substances Data)

Usage

Description

[1,1-Biphenyl]-3,4,4-triol (9CI), also known as biphenyl triol, is a phenolic chemical compound characterized by a biphenyl backbone with three hydroxyl groups attached to it. [1,1-Biphenyl]-3,4,4-triol (9CI) exhibits potential antioxidant and anti-inflammatory properties, making it a promising candidate for pharmaceutical and therapeutic applications. The hydroxyl groups present in its structure enable it to act as a potent scavenger of free radicals, which are known to contribute to oxidative stress and various diseases.

Uses

Used in Pharmaceutical Industry:
[1,1-Biphenyl]-3,4,4-triol (9CI) is used as a potential therapeutic agent for its antioxidant and anti-inflammatory properties. [1,1-Biphenyl]-3,4,4-triol (9CI)'s ability to protect cells and tissues from oxidative damage and inflammation makes it a valuable candidate for the development of new drugs targeting conditions related to oxidative stress and inflammation.
Used in Antioxidant Applications:
In the field of antioxidant research, [1,1-Biphenyl]-3,4,4-triol (9CI) is utilized for its potential to neutralize free radicals, which are major contributors to oxidative stress and the development of various diseases. Its unique chemical structure allows it to effectively scavenge these harmful molecules, providing a protective effect against oxidative damage.
Used in Research and Development:
[1,1-Biphenyl]-3,4,4-triol (9CI) is employed as a key compound in scientific research, particularly in the study of its antioxidant and anti-inflammatory properties. Researchers use this compound to investigate its potential applications in the development of new pharmaceuticals and therapeutic strategies for treating diseases associated with oxidative stress and inflammation.

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Relevant articles and documents

Conversion of Simple Cyclohexanones into Catechols

A novel I2-catalyzed direct conversion of cyclohexanones to substituted catechols under mild and simple conditions has been described. This novel transformation is remarkable with the multiple oxygenation and dehydrogenative aromatization processes enabled just by using DMSO as the solvent, oxidant, and oxygen source. This metal-free and simple system demonstrates a versatile protocol for the synthesis of highly valuable substituted catechols and therefore streamlines the synthesis and modification of biologically important molecules for drug discovery.