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Catalog Number:
40388
CAS Number:
227305-69-3
Ácido 2,3-dihidrobenzofurano-5-borónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
2,3-Dihidrobenzo[b]furano-5-borónico, Ácido 2,3-dihidro-1-benzofuran-5-ilborónico
Documents
$161.64 /200 mg
Tamaño
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Información del producto

2,3-Dihydrobenzofuran-5-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 development of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a benzofuran moiety, enhances its reactivity and selectivity in various chemical transformations, providing researchers with a powerful tool for synthesizing diverse compounds.

In addition to its synthetic applications, 2,3-Dihydrobenzofuran-5-boronic acid has shown potential in the development of biologically active molecules, particularly in the field of drug discovery. Its boronic acid functionality allows for the formation of reversible covalent bonds with diols, which is advantageous in designing inhibitors and other therapeutic agents. This compound's ability to facilitate the creation of novel structures while maintaining high specificity makes it a valuable asset for researchers and industry professionals aiming to innovate in their respective fields.

Número CAS
227305-69-3
Fórmula molecular
C8H9BO3
Peso molecular
163.97
Número MDL
MFCD02681979
Punto de fusión
240 °C (Literatura)
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
227305-69-3
Fórmula molecular
C8H9BO3
Peso molecular
163.97
Número MDL
MFCD02681979
Punto de fusión
240 °C (Literatura)
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

2,3-Dihydrobenzofuran-5-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing treatments for neurological disorders.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for creating complex organic molecules, making it valuable in the production of agrochemicals and fine chemicals.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, facilitating the development of targeted drug delivery systems in biomedical applications.
  • Material Science: It is used in the formulation of advanced materials, including sensors and polymers, due to its unique chemical properties that enhance material performance.
  • Analytical Chemistry: This compound is beneficial in the development of analytical methods for detecting specific biomolecules, aiding in diagnostics and research in biochemistry.

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