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Catalog Number:
28658
CAS Number:
452972-09-7
Ácido 5-bromopiridina-3-borónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido (5-bromo-3-piridinil)borónico
Documents
$45.47 /1G
Tamaño
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Información del producto

5-Bromopyridine-3-boronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of various biaryl compounds, which are significant in pharmaceuticals and agrochemicals. Its unique bromine substituent enhances its reactivity and selectivity, allowing for the development of complex molecular architectures. Researchers and industry professionals utilize 5-Bromopyridine-3-boronic acid in the design of targeted therapies and in the creation of novel materials, particularly in the fields of drug discovery and material science.

The compound's solubility in common organic solvents and its stability under standard laboratory conditions further enhance its appeal for laboratory applications. Its compatibility with a range of functional groups allows for diverse synthetic pathways, making it a valuable asset in both academic research and industrial applications. With its proven efficacy in facilitating complex reactions, 5-Bromopyridine-3-boronic acid stands out as a key reagent for those looking to innovate in chemical synthesis.

Número CAS
452972-09-7
Fórmula molecular
C5H5BBrNO2
Peso molecular
201.81
Número MDL
MFCD02685634
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
452972-09-7
Fórmula molecular
C5H5BBrNO2
Peso molecular
201.81
Número MDL
MFCD02685634
Condiciones
Conservar entre 0 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
-
Aplicaciones

5-Bromopyridine-3-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is crucial in synthesizing various pharmaceuticals, particularly in creating targeted therapies for diseases like cancer. Its boronic acid functionality allows for the formation of stable complexes with biomolecules.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, facilitating the development of complex organic molecules. Researchers often use it in Suzuki coupling reactions, which are essential for creating carbon-carbon bonds.
  • Agricultural Chemistry: The compound is explored for its potential in developing agrochemicals, including herbicides and pesticides, which can enhance crop protection and yield.
  • Material Science: It is applied in the creation of advanced materials, such as polymers and nanomaterials, where its unique properties can improve material performance and functionality.
  • Diagnostic Tools: The compound is being investigated for use in diagnostic applications, particularly in the development of sensors that can detect specific biomolecules, aiding in early disease detection.

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