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Catalog Number:
40303
CAS Number:
871329-82-7
Acide 3-fluoro-5-hydroxyphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-fluoro-5-hydroxybenzèneboronique
Documents
$118.08 /1G
Taille
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Informations sur le produit

3-Fluoro-5-hydroxyphenylboronic acid is a versatile compound that plays a crucial role in various fields, particularly in medicinal chemistry and organic synthesis. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of pharmaceuticals and agrochemicals. Its unique fluorine substitution enhances its reactivity and selectivity, allowing for precise modifications in chemical reactions. Researchers often utilize this compound in the synthesis of biologically active molecules, including potential drug candidates, due to its favorable properties.

In addition to its applications in drug discovery, 3-Fluoro-5-hydroxyphenylboronic acid is also employed in the development of sensors and materials science. Its ability to interact with various substrates makes it a valuable tool in the design of innovative materials with tailored properties. The compound's stability and compatibility with diverse reaction conditions further enhance its utility in both academic and industrial settings. By incorporating this compound into your research or production processes, you can leverage its unique characteristics to achieve superior results.

Numéro CAS 
871329-82-7
Formule moléculaire
C 6 H 6 BFO 3
Poids moléculaire 
155.92
Point de fusion 
62 °C (lit.)
Informations générales
Numéro CAS 
871329-82-7
Formule moléculaire
C 6 H 6 BFO 3
Poids moléculaire 
155.92
Point de fusion 
62 °C (lit.)
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

3-Fluoro-5-hydroxyphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of pharmaceuticals, particularly in developing anti-cancer agents. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies and diagnostic tools in the biomedical field.
  • Organic Synthesis: Researchers employ this compound in organic synthesis reactions, particularly in cross-coupling reactions, to create complex organic molecules efficiently, which is valuable in materials science.
  • Fluorescent Probes: Its unique properties allow it to be used in developing fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Environmental Monitoring: This chemical can be utilized in the detection of phenolic compounds in environmental samples, helping industries comply with regulations and ensuring environmental safety.

Citations