Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
40381
CAS Number:
162607-15-0
Ácido 4-metil-2-tiofenoborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-metiltiofeno-2-borónico
Documents
$75.11 /1G
Tamaño
Request Bulk Quote
Información del producto

4-Methyl-2-thiopheneboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its unique ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of various biaryl compounds. Its distinctive thiophene ring enhances its electronic properties, allowing for improved reactivity and selectivity in coupling reactions. Researchers and industry professionals can leverage this compound in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular structures are crucial.

In addition to its synthetic applications, 4-Methyl-2-thiopheneboronic acid has shown promise in the field of sensor technology, particularly in the detection of biomolecules. Its functional properties enable the design of sensitive and selective sensors, which can be pivotal in medical diagnostics and environmental monitoring. The compound's stability and ease of handling further enhance its appeal, making it a valuable asset in both laboratory and industrial settings.

Número CAS
162607-15-0
Fórmula molecular
C5H7BO2S
Peso molecular
141.98
Número MDL
MFCD01319040
Punto de fusión
125-126 °C
Densidad
1,30 g/ml
Índice de refracción
n20D 1,55
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
162607-15-0
Fórmula molecular
C5H7BO2S
Peso molecular
141.98
Número MDL
MFCD01319040
Punto de fusión
125-126 °C
Densidad
1,30 g/ml
Índice de refracción
n20D 1,55
Condiciones
Conservar entre 2 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

4-Methyl-2-thiopheneboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, allowing researchers to create complex carbon-carbon bonds, which are essential in the formation of advanced materials.
  • Sensor Development: The unique properties of this boronic acid make it ideal for developing sensors that detect sugars and other biomolecules, benefiting the food and healthcare industries.
  • Material Science: It is employed in the creation of conductive polymers and materials, enhancing the performance of electronic devices and renewable energy technologies.
  • Medicinal Chemistry: Researchers utilize it in drug discovery processes, particularly for targeting specific biological pathways, leading to more effective treatments with fewer side effects.

Citas