482628-23-9

Basic information

• Product Name: (4-Fluoro-3,5-dimethoxyphenyl)boronic acid
• Synonyms: (4-Fluoro-3,5-dimethoxyphenyl)boronic acid
• CAS NO: 482628-23-9
• Molecular Formula: C₈H₁₀BFO₄
• Molecular Weight: 199.9720032
• Mol File: 482628-23-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: (4-Fluoro-3,5-dimethoxyphenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-Fluoro-3,5-dimethoxyphenyl)boronic acid(482628-23-9)
• EPA Substance Registry System: (4-Fluoro-3,5-dimethoxyphenyl)boronic acid(482628-23-9)

Safety Data

• Hazardous Substances Data: 482628-23-9(Hazardous Substances Data)

Usage

Description

(4-fluoro-3,5-dimethoxyphenyl)boronic acid is a chemical compound that features a boronic acid functional group attached to a phenyl ring, which is substituted with a fluorine atom and two methoxy groups. This unique structure endows it with specific reactivity and selectivity, making it a valuable component in various chemical and pharmaceutical applications.

Uses

Used in Organic Synthesis:
(4-fluoro-3,5-dimethoxyphenyl)boronic acid serves as a reagent in organic synthesis, where it is utilized for the formation of carbon-carbon and carbon-heteroatom bonds. Its presence facilitates the creation of complex organic molecules, contributing to the advancement of chemical research.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-fluoro-3,5-dimethoxyphenyl)boronic acid is applied as a building block for the development of new drugs. Its unique structure allows for the design of molecules with potential therapeutic properties, such as anti-cancer and anti-inflammatory agents.
Used in Drug Discovery:
(4-fluoro-3,5-dimethoxyphenyl)boronic acid is also used in drug discovery processes, where its mild and selective reactivity is advantageous. It aids in the construction of diverse chemical compounds that can be further explored for their pharmaceutical potential.
Used in the Synthesis of Complex Organic Molecules:
Due to its versatile nature, (4-fluoro-3,5-dimethoxyphenyl)boronic acid is employed in the synthesis of complex organic molecules. This application is crucial for expanding the library of chemical compounds available for various industrial and research purposes.

Downstream Products

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