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Catalog Number:
40260
CAS Number:
149507-26-6
Ácido 3-fluoro-4-metoxifenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 3-fluoro-4-metoxibencenoborónico
Documents
$40.96 /1G
Tamaño
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Información del producto

3-Fluoro-4-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the development of complex organic molecules. Its unique fluorine and methoxy substituents enhance its reactivity and selectivity, making it an excellent choice for researchers looking to synthesize pharmaceuticals, agrochemicals, and advanced materials.

In addition to its synthetic applications, 3-Fluoro-4-methoxyphenylboronic acid has shown potential in the development of targeted therapies, particularly in the field of cancer research, where it can be used to create compounds that inhibit specific biological pathways. Its stability and compatibility with various reaction conditions further underscore its importance in both academic and industrial settings. Researchers and industry professionals will find this compound to be a reliable building block for innovative chemical synthesis and drug discovery.

Número CAS
149507-26-6
Fórmula molecular
C7H8BFO3
Peso molecular
169.95
Número MDL
MFCD00807404
Punto de fusión
198 °C (dec.)
Condiciones
Tienda en RT
Información general
Número CAS
149507-26-6
Fórmula molecular
C7H8BFO3
Peso molecular
169.95
Número MDL
MFCD00807404
Punto de fusión
198 °C (dec.)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

3-Fluoro-4-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and diabetes.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, allowing for the construction of complex organic molecules with precision and efficiency.
  • Material Science: The compound is used in the creation of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation processes for labeling biomolecules in research and diagnostics.
  • Analytical Chemistry: It is utilized in sensor technology for detecting glucose and other biomolecules, providing a reliable method for monitoring health conditions.

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