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Catalog Number:
40360
CAS Number:
868662-36-6
Ácido 2-(trifluorometil)piridina-5-borónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 6-(trifluorometil)-3-piridilborónico
Documents
$112.57 /1G
Tamaño
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Información del producto

2-(Trifluoromethyl)pyridine-5-boronic 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 coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances lipophilicity, which can improve the bioavailability of drug candidates, thereby making it a crucial component in the development of new therapeutic agents.

Researchers and industry professionals appreciate this compound for its unique reactivity and stability, which allows for the formation of carbon-carbon bonds under mild conditions. Its application extends to the development of advanced materials and fine chemicals, where precision and efficiency are paramount. With its favorable properties, 2-(Trifluoromethyl)pyridine-5-boronic acid stands out as a key reagent for innovative research and development in various fields, including pharmaceuticals, agrochemicals, and materials science.

Número CAS
868662-36-6
Fórmula molecular
C6H5BF3NO2
Peso molecular
190.92
Número MDL
MFCD07375381
Condiciones
Tienda en RT
Información general
Número CAS
868662-36-6
Fórmula molecular
C6H5BF3NO2
Peso molecular
190.92
Número MDL
MFCD07375381
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

2-(Trifluoromethyl)pyridine-5-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 creating compounds that target specific biological pathways, enhancing drug efficacy.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki reactions, to form carbon-carbon bonds, which are essential in building complex organic molecules.
  • Agricultural Chemistry: This chemical is used in the development of agrochemicals, including herbicides and pesticides, providing effective solutions for crop protection and yield enhancement.
  • Material Science: It plays a role in the formulation of advanced materials, including polymers and coatings, due to its unique electronic properties, which can improve material performance.
  • Analytical Chemistry: The compound is utilized in various analytical techniques for detecting and quantifying other substances, making it valuable in quality control and environmental monitoring.

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