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Catalog Number:
40381
CAS Number:
162607-15-0
Acide 4-méthyl-2-thiophèneboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-méthylthiophène-2-boronique
Documents
$75.11 /1G
Taille
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Informations sur le produit

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.

Numéro CAS 
162607-15-0
Formule moléculaire
C 5 H 7 B O 2 S
Poids moléculaire 
141.98
Point de fusion 
125 - 126 °C
Indice de réfraction 
n20D 1,55
Informations générales
Numéro CAS 
162607-15-0
Formule moléculaire
C 5 H 7 B O 2 S
Poids moléculaire 
141.98
Point de fusion 
125 - 126 °C
Indice de réfraction 
n20D 1,55
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

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.

Citations