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Catalog Number:
40394
CAS Number:
4347-33-5
Acide 5-formyl-2-thiophèneboronique
Purity:
≥ 96 % (HPLC)
Synonym(s):
Acide 5-formyl-2-thiénylboronique
Documents
$18.53 /1G
Taille
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Informations sur le produit

5-Formyl-2-thiopheneboronic acid is a versatile compound recognized for its unique properties and applications in organic synthesis and medicinal chemistry. This boronic acid derivative features a thiophene ring, which enhances its reactivity and makes it an excellent building block for the development of various organic molecules. Its ability to form stable complexes with diols and other Lewis bases allows it to play a crucial role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds essential for creating complex organic structures.

Researchers and industry professionals can leverage 5-Formyl-2-thiopheneboronic acid in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its application in the preparation of biologically active compounds, such as anti-cancer agents and other therapeutic drugs, highlights its significance in drug discovery and development. Moreover, its compatibility with various reaction conditions makes it a preferred choice for chemists seeking efficient and reliable reagents in their synthetic pathways.

Numéro CAS 
4347-33-5
Formule moléculaire
C 5 H 5 B O 3 S
Poids moléculaire 
155.96
Point de fusion 
132 - 135 °C
Informations générales
Numéro CAS 
4347-33-5
Formule moléculaire
C 5 H 5 B O 3 S
Poids moléculaire 
155.96
Point de fusion 
132 - 135 °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-Formyl-2-thiopheneboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key 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 biologically active compounds, making it valuable in medicinal chemistry for designing new drugs.
  • Material Science: Used in the production of conductive polymers and organic electronics, it enhances the performance of materials in devices like solar cells and sensors.
  • Catalysis: This compound acts as a catalyst in various chemical reactions, improving efficiency and selectivity in processes such as cross-coupling reactions.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.

Citations