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Catalog Number:
40384
CAS Number:
917471-30-8
Ácido 5-(1-propinil)piridina-3-borónico
Purity:
98 - 105% (Ensayo por titulación)
Synonym(s):
Ácido B-[5-(1-propin-1-il)-3-piridinil]-borónico
Documents
$375.36 /1G
Tamaño
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Información del producto

5-(1-Propynyl)pyridine-3-boronic 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 Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to facilitate the development of complex organic molecules, including pharmaceuticals and agrochemicals. Its application extends to the synthesis of biologically active compounds, where it serves as a key building block in the creation of targeted therapies.

The compound's distinct structural features allow for enhanced reactivity and selectivity in various chemical transformations. Its role in the synthesis of advanced materials and fine chemicals highlights its importance in both academic research and industrial applications. With its proven efficacy in facilitating efficient reactions, 5-(1-Propynyl)pyridine-3-boronic acid stands out as a valuable tool for chemists aiming to innovate and streamline their synthetic processes.

Número CAS
917471-30-8
Fórmula molecular
C8H8BNO2
Peso molecular
160.97
Número MDL
MFCD18258851
Condiciones
Tienda en RT
Información general
Número CAS
917471-30-8
Fórmula molecular
C8H8BNO2
Peso molecular
160.97
Número MDL
MFCD18258851
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

5-(1-Propynyl)pyridine-3-boronic 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 anti-cancer agents due to its ability to form stable complexes with biomolecules.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura reactions, to create complex organic molecules, making it invaluable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the creation of functional materials, including sensors and catalysts, thanks to its unique electronic properties and ability to form strong bonds with other materials.
  • Bioconjugation: It is utilized in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating advancements in drug delivery systems and diagnostic tools.
  • Research in Catalysis: This boronic acid derivative plays a significant role in catalytic processes, enhancing reaction efficiency and selectivity, which is crucial for sustainable chemistry practices.

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