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Catalog Number:
40344
CAS Number:
154549-38-9
Ácido 2,4,6-triisopropilfenilborónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 2,4,6-triisopropilbencenoborónico
Documents
$68.20 /1G
Tamaño
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Información del producto

2,4,6-Triisopropylphenylboronic acid is a versatile organoboron compound recognized for its significant role in organic synthesis and medicinal chemistry. This compound features a triisopropylphenyl group, which enhances its solubility and stability, making it an excellent choice for various applications. It is particularly useful in Suzuki-Miyaura coupling reactions, a fundamental method for forming carbon-carbon bonds, which is essential in the development of pharmaceuticals and agrochemicals. Additionally, its unique structure allows for selective binding in biological systems, making it a valuable tool in drug discovery and development.

Researchers and industry professionals appreciate 2,4,6-Triisopropylphenylboronic acid for its efficiency in facilitating complex organic transformations while minimizing by-products. Its robust nature and compatibility with various reaction conditions make it a preferred choice for those looking to streamline their synthetic pathways. With its potential to enhance reaction yields and simplify purification processes, this compound stands out in the field of synthetic organic chemistry.

Número CAS
154549-38-9
Fórmula molecular
C 15 H 25 BO 2
Peso molecular
248.17
Número MDL
MFCD02683099
Punto de fusión
165 °C (descenso)
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
154549-38-9
Fórmula molecular
C 15 H 25 BO 2
Peso molecular
248.17
Número MDL
MFCD02683099
Punto de fusión
165 °C (descenso)
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

2,4,6-Triisopropylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the formation of complex molecules through Suzuki coupling reactions, which are essential for creating pharmaceuticals and agrochemicals.
  • Drug Development: In medicinal chemistry, it plays a crucial role in the design of boron-containing drugs, which can enhance the efficacy and selectivity of therapeutic agents, particularly in cancer treatment.
  • Material Science: It is used in the development of advanced materials, such as polymers and nanomaterials, where its unique properties can improve mechanical strength and thermal stability.
  • Bioconjugation: The compound is valuable in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for diagnostics and targeted drug delivery systems.
  • Environmental Applications: It can be utilized in the detection and removal of pollutants, as its boronic acid functionality can selectively bind to certain environmental contaminants, aiding in water purification processes.

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