製品名:3-Fluoro-4-biphenylboronic acid

IUPAC Name:{3-fluoro-[1,1'-biphenyl]-4-yl}boronic acid

CAS番号:409108-13-0
分子式:C12H10BFO2
純度:95%
カタログ番号:CM136891
分子量:216.02

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製品詳細

CAS番号:409108-13-0
分子式:C12H10BFO2
融点:-
SMILESコード:OB(C1=CC=C(C2=CC=CC=C2)C=C1F)O
密度:
カタログ番号:CM136891
分子量:216.02
沸点:
MDL番号:MFCD04115668
保管方法:

Category Infos

Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Product Overview 3-Fluoro-4-biphenylboronic acid (409108-13-0) is a type of organic compound with a boronic acid group and two phenyl groups. It is a useful reagent in organic synthesis, as it can be used to form a variety of compounds, such as carboxylic acids, amides, and esters. 3-Fluoro-4-biphenylboronic acid is also used in scientific research as a chemical probe to study the structure and function of proteins and other biomolecules.
Physical Properties 3-Fluoro-4-biphenylboronic acid is a white solid with a melting point of around 237-242°C.
Chemical Properties 3-Fluoro-4-biphenylboronic acid is a reactive compound, often utilized as a starting material or intermediate in various chemical reactions and synthesis processes.
Synthesis and Application 3-Fluoro-4-biphenylboronic acid has been used in scientific research as a chemical probe to study the structure and function of proteins and other biomolecules. It has been used to study the structure of proteins, such as the enzyme acetylcholinesterase, and the function of proteins, such as the enzyme monoamine oxidase. In addition, 3-Fluoro-4-biphenylboronic acid has been used to study the structure and function of other biomolecules, such as DNA and RNA.
Storage and Handling Sealed in dry at 2-8°C.