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Catalog Number:
40272
CAS Number:
123291-97-4
Ácido 2-etoxi-5-metilfenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 2-etoxi-5-metilbencenoborónico
Documents
$105.56 /1G
Tamaño
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Información del producto

2-Ethoxy-5-methylphenylboronic acid is a versatile boronic acid derivative known for its significant role in organic synthesis and medicinal chemistry. This compound features a unique structure that allows it to participate in various cross-coupling reactions, making it an essential reagent for the formation of carbon-carbon bonds. Its ability to selectively bind to diols enhances its utility in the development of complex organic molecules, particularly in the synthesis of pharmaceuticals and agrochemicals. Researchers appreciate its effectiveness in Suzuki-Miyaura coupling reactions, where it facilitates the formation of aryl-aryl bonds, crucial for creating diverse chemical libraries.

In addition to its synthetic applications, 2-Ethoxy-5-methylphenylboronic acid is recognized for its potential in the development of targeted therapies, particularly in cancer research. Its boron atom can interact with biological molecules, opening avenues for innovative drug design. The compound's stability and ease of handling make it a preferred choice for both academic and industrial laboratories. With its broad applicability and unique properties, 2-Ethoxy-5-methylphenylboronic acid stands out as a valuable tool for chemists seeking to advance their research and development projects.

Número CAS
123291-97-4
Fórmula molecular
C 9 H 13 BO 3
Peso molecular
180.01
Número MDL
MFCD00196832
Punto de fusión
94 °C (Literatura)
Condiciones
Tienda en RT
Información general
Número CAS
123291-97-4
Fórmula molecular
C 9 H 13 BO 3
Peso molecular
180.01
Número MDL
MFCD00196832
Punto de fusión
94 °C (Literatura)
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-Ethoxy-5-methylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, allowing chemists to form carbon-carbon bonds efficiently, which is essential in creating various organic compounds.
  • Drug Development: The compound is significant in medicinal chemistry for designing and optimizing drug candidates, particularly in targeting specific biological pathways.
  • Material Science: It is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and strength.
  • Bioconjugation: This chemical facilitates the attachment of biomolecules to surfaces or other molecules, which is vital in creating biosensors and targeted drug delivery systems.

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