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Catalog Number:
40386
CAS Number:
62306-79-0
Ácido 5-metil-2-furanborónico
Purity:
96 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 5-metil-2-furilborónico
Documents
$88.93 /1G
Tamaño
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Información del producto

5-Methyl-2-furanboronic acid is a versatile boronic acid derivative that plays a significant role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds. Its unique furan ring structure enhances its reactivity and compatibility with various substrates, allowing for the development of complex molecules in pharmaceutical research. Additionally, 5-Methyl-2-furanboronic acid serves as a key intermediate in the synthesis of biologically active compounds, including potential drug candidates, thereby supporting advancements in therapeutic applications.

Researchers and industry professionals can leverage the properties of 5-Methyl-2-furanboronic acid for the development of novel materials and pharmaceuticals. Its ease of use in synthetic pathways and the ability to fine-tune molecular properties make it an attractive choice for those looking to innovate in chemical synthesis. With its growing relevance in the field, this compound stands out as a crucial tool for enhancing research outcomes and driving forward the development of new chemical entities.

Número CAS
62306-79-0
Fórmula molecular
C5H7BO3
Peso molecular
125.92
Número MDL
MFCD01114644
Punto de fusión
82 °C (Literatura)
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
62306-79-0
Fórmula molecular
C5H7BO3
Peso molecular
125.92
Número MDL
MFCD01114644
Punto de fusión
82 °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

5-Methyl-2-furanboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex carbon-carbon bonds efficiently, which is essential in drug discovery.
  • Sensor Development: The unique properties of this boronic acid make it suitable for developing chemical sensors, particularly for detecting sugars and other biomolecules, enhancing biosensing technologies.
  • Material Science: It is utilized in the formulation of advanced materials, including polymers and coatings, due to its ability to modify the physical properties of materials, leading to improved performance.
  • Medicinal Chemistry: Researchers leverage its reactivity to design and optimize drug candidates, particularly in targeting specific biological pathways, which can lead to more effective treatments.

Citas