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Catalog Number:
40262
CAS Number:
872460-12-3
Ácido 3-carboxi-4-fluorofenilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 3-carboxi-4-fluorobencenoborónico
Documents
$93.14 /1G
Tamaño
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Información del producto

3-Carboxy-4-fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique fluorine substitution enhances its reactivity and selectivity in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, which is pivotal for constructing complex organic molecules. Researchers appreciate its role in the synthesis of biologically active compounds, including potential anticancer agents and other therapeutic molecules.

In addition to its synthetic applications, 3-Carboxy-4-fluorophenylboronic acid serves as a valuable tool in the field of materials science, particularly in the development of sensors and polymers. Its ability to interact with carbohydrates and other biomolecules opens avenues for innovative applications in biosensing and drug delivery systems. With its favorable properties and broad applicability, this compound stands out as a key ingredient for researchers and industry professionals aiming to advance their projects in organic synthesis and material development.

Número CAS
872460-12-3
Fórmula molecular
C 7 H 6 BFO 4
Peso molecular
183.93
Número MDL
MFCD03095129
Punto de fusión
219 °C (Literatura)
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
872460-12-3
Fórmula molecular
C 7 H 6 BFO 4
Peso molecular
183.93
Número MDL
MFCD03095129
Punto de fusión
219 °C (Literatura)
Condiciones
Conservar entre 2 y 8 °C.
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

3-Carboxy-4-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 development of drugs targeting cancer and diabetes. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Organic Synthesis: It is a valuable reagent in organic chemistry for the construction of complex molecules. Researchers use it in Suzuki coupling reactions, which are essential for creating biaryl compounds found in many natural products and pharmaceuticals.
  • Material Science: This chemical is used in the development of advanced materials, such as polymers and nanomaterials. Its unique properties allow for the modification of material surfaces, improving their performance in various applications.
  • Bioconjugation: In biochemistry, it is employed for labeling biomolecules. The boronic acid group can selectively bind to diols, making it useful for creating targeted drug delivery systems and diagnostic tools.
  • Environmental Monitoring: This compound can be utilized in the detection of environmental pollutants. Its chemical properties allow for the development of sensors that can identify specific contaminants in water and soil, contributing to environmental protection efforts.

Citas