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Catalog Number:
40377
CAS Number:
206551-43-1
Acide 5-acétyl-2-thiophèneboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide (2-acétylthién-5-yl)boronique, Acide (5-acétylthién-2-yl)boronique, Acide 5-acétyl-2-thiophèneboronique
Documents
$83.42 /5G
Taille
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Informations sur le produit

5-Acetyl-2-thiopheneboronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with various substrates, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals utilize this compound for the development of pharmaceuticals, agrochemicals, and advanced materials due to its unique electronic properties and functionalization potential. Its application in the synthesis of biologically active molecules highlights its importance in drug discovery and development, particularly in creating compounds with enhanced efficacy and selectivity.

Moreover, 5-Acetyl-2-thiopheneboronic acid stands out for its compatibility with a range of reaction conditions, allowing for greater flexibility in synthetic pathways. This characteristic, combined with its relatively straightforward preparation, positions it as a preferred choice for chemists looking to streamline their workflows. Whether you are involved in academic research or industrial applications, this compound offers significant advantages in efficiency and effectiveness, making it a valuable addition to your chemical toolkit.

Numéro CAS 
206551-43-1
Formule moléculaire
C 6 H 7 BO 3 S
Poids moléculaire 
169.99
Point de fusion 
133 - 138 °C
Informations générales
Numéro CAS 
206551-43-1
Formule moléculaire
C 6 H 7 BO 3 S
Poids moléculaire 
169.99
Point de fusion 
133 - 138 °C
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

5-Acetyl-2-thiopheneboronic 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.
  • Drug Development: Its unique boronic acid functionality allows for the creation of targeted drug delivery systems, enhancing the efficacy of therapeutic agents in treating diseases such as cancer.
  • Material Science: It is employed in the fabrication of advanced materials, including conductive polymers and sensors, due to its ability to form stable complexes with metals.
  • Biochemistry: In biochemical research, this compound is used to study enzyme interactions and mechanisms, particularly in the context of protease inhibitors.
  • Environmental Chemistry: It plays a role in the development of sensors for detecting environmental pollutants, contributing to efforts in monitoring and improving environmental health.

Citations