301823-87-0

Basic information

• Product Name: [1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI)
• Synonyms: [1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI)
• CAS NO: 301823-87-0
• Molecular Formula: C12H10O6
• Molecular Weight: 250.2
• Product Categories: BIPHENYL
• Mol File: 301823-87-0.mol

Chemical Properties

• Melting Point: >300 °C
• Boiling Point: 580.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.721±0.06 g/cm3(Predicted)
• PKA: 8.84±0.45(Predicted)
• CAS DataBase Reference: [1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI)(301823-87-0)
• EPA Substance Registry System: [1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI)(301823-87-0)

Safety Data

• Hazardous Substances Data: 301823-87-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Applications:
[1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI) is used as a chemical intermediate for the development of pharmaceutical compounds. Its unique structure with multiple hydroxy groups allows for the creation of various derivatives with potential therapeutic properties.
Used in Materials Science:
In the field of materials science, [1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI) is used as a building block for the synthesis of novel materials with specific properties. Its ability to form hydrogen bonds and its structural characteristics make it a valuable component in the development of advanced materials.
Used in Organic Synthesis:
[1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI) serves as a key intermediate in organic synthesis, where it can be further modified to produce a range of organic compounds with diverse applications. Its versatility in chemical reactions makes it a valuable asset in the synthesis of complex organic molecules.
Used in Scientific Research:
[1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI) is also utilized in scientific research to study its properties, reactivity, and potential applications. Researchers may use [1,1-Biphenyl]-2,3,3,4,4,5-hexol(9CI) to explore new reaction pathways, investigate its interactions with other molecules, and understand its potential role in various chemical processes.

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Relevant articles and documents

Catalytic aerobic oxidative coupling of some simple phenols and natural phenanthrols with CuCl(OH).TMEDA

Aerobic oxidative coupling of phenol, catechol, resorcinol and pyrogallol with CuCl(OH).TMEDA as catalyst affords 2',4-dihydroxybiphenyl (1a), 3,3',4,4'-tetrahydroxybiphenyl (2a), 2,2',4,4'-tetrahydroxybiphenyl (3a) and 2,2',4,6'-tetrahydroxybiphenyl (4a) and 2',3,3',4,4',5-hexahydroxybiphenyl (5a), respectively, in moderate yields. Similar catalytic aerobic oxidative coupling of the naturally occurring phenanthrols, nudol (6a) [2,7-dihydroxy-3,4-dimethoxyphenanthrene], 2,7-dihydroxy-3,4,6-trimethoxyphenanthrene (6b) and cirrhopetalin (7) [7-hydroxy-4-methoxy-2,3-methylenedioxyphenanthrene] with the same reagent gives the corresponding 1,1'-biphenanthryls 8a and 8c and the 8,8'-biphenanthryl 9a, respectively, in very good yields. All these reactions exhibit a high degree of regioselectivity.