3871-23-6

Basic information

• Product Name: [1,1'-Biphenyl]-4-ol, phosphate (3:1)
• CAS NO: 3871-23-6
• Molecular Formula: C36H27O4P
• Molecular Weight: 554.582
• Mol File: 3871-23-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: [1,1'-Biphenyl]-4-ol, phosphate (3:1)(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1'-Biphenyl]-4-ol, phosphate (3:1)(3871-23-6)
• EPA Substance Registry System: [1,1'-Biphenyl]-4-ol, phosphate (3:1)(3871-23-6)

Safety Data

• Hazardous Substances Data: 3871-23-6(Hazardous Substances Data)

Usage

General Description

[1,1'-Biphenyl]-4-ol, phosphate (3:1) is a chemical compound that consists of a phosphate group and a [1,1'-Biphenyl]-4-ol molecule in a 3:1 ratio. [1,1'-Biphenyl]-4-ol, phosphate (3:1) is often used in the production of flame retardants and as a stabilizer in industrial processes. It has also been found to have potential applications in the field of pharmaceuticals and agrochemicals. The phosphate group in the compound allows it to be easily incorporated into polymers and other materials, making it useful for creating flame-resistant products. Additionally, the [1,1'-Biphenyl]-4-ol component of the compound has antioxidant properties, making it beneficial for use in various industrial applications. Overall, [1,1'-Biphenyl]-4-ol, phosphate (3:1) is a versatile chemical with a range of potential uses across different industries.

Upstream product

• 25963-45-5 tris(([1,1'-biphenyl]-4-yl)) phosphite 
• 92-69-3 4-Phenylphenol 
• 108-95-2 phenol 
• 3645-61-2 sodium 4-phenylphenoxide 

Relevant articles and documents

Diphenyl Diselenide-Catalyzed Synthesis of Triaryl Phosphites and Triaryl Phosphates from White Phosphorus

Industrially important triaryl phosphites, traditionally prepared from PCl3, have been synthesized by a diphenyl diselenide-catalyzed one-step procedure involving white phosphorus and phenols, which provides a halogen- and transition metal-free way to these compounds. Subsequent oxidation of triaryl phosphites produces triaryl phosphates and triaryl thiophosphates. Phosphorotrithioates are also prepared efficiently from aromatic thiols and aliphatic thiols.

Process for producing triaryl phosphate

A process for producing triaryl phosphate, comprising reacting at least one specific aromatic hydroxy compound with phosphorus pentachloride to form a chlorophosphorane compound and reacting water, an alcohol, an alcohol aqueous solution or an alkaline aqueous solution with the chlorophosphorane compound. The process permits the production of triaryl phosphate at high yields at a low temperature for a relatively short period of time, making the removal and treatment of a catalyst simply and obviating the use of the catalyst in some cases.

Synthesis of Triaryl Phosphates via Phase-Transfer Catalysis

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