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Catalog Number:
40309
CAS Number:
137504-86-0
Ácido 4-cloro-3-fluorofenilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-cloro-3-fluorobencenoborónico
Documents
$27.94 /1G
Tamaño
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Información del producto

4-Chloro-3-fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique combination of chlorine and fluorine substituents enhances its reactivity and selectivity, allowing researchers to create compounds with specific properties tailored to their applications.

In addition to its role in synthetic chemistry, 4-Chloro-3-fluorophenylboronic acid has shown potential in the development of targeted therapies, particularly in the field of cancer research. Its ability to form stable complexes with various substrates makes it a valuable tool for drug discovery and development. Researchers can leverage its properties to explore new therapeutic avenues, making it an indispensable asset in both academic and industrial laboratories.

Número CAS
137504-86-0
Fórmula molecular
C6H5BClFO2
Peso molecular
174.36
Número MDL
MFCD01319010
Punto de fusión
144 °C (Literatura)
Condiciones
Tienda en RT
Información general
Número CAS
137504-86-0
Fórmula molecular
C6H5BClFO2
Peso molecular
174.36
Número MDL
MFCD01319010
Punto de fusión
144 °C (Literatura)
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
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Aplicaciones

4-Chloro-3-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in the synthesis of various pharmaceuticals, particularly in the creation of targeted therapies for cancer treatment.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, enabling the formation of complex molecules through cross-coupling reactions, which are essential in creating new materials.
  • Bioconjugation: The compound is used to attach biomolecules in bioconjugation processes, enhancing drug delivery systems and improving the efficacy of therapeutic agents.
  • Sensor Technology: It is applied in the development of chemical sensors, particularly for detecting specific ions or molecules, which is valuable in environmental monitoring and safety applications.
  • Research in Material Science: This boronic acid derivative is utilized in the development of advanced materials, including polymers and nanomaterials, which have applications in electronics and nanotechnology.

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