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Catalog Number:
40326
CAS Number:
127972-00-3
Acide 2-méthoxy-5-méthylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-méthoxy-5-méthylbenzèneboronique
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$111.17 /5G
Taille
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Informations sur le produit

2-Methoxy-5-methylphenylboronic acid is a versatile organoboron compound that plays a crucial role in various chemical synthesis applications. This compound is particularly valued in the field of medicinal chemistry for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers utilize this compound to facilitate the formation of carbon-carbon bonds, which is fundamental in the development of pharmaceuticals and agrochemicals. Its unique structure allows for selective reactivity, enhancing the efficiency of synthetic pathways while minimizing by-products.

In addition to its applications in organic synthesis, 2-Methoxy-5-methylphenylboronic acid is also employed in the development of sensors and materials science, where its boronic acid functionality can interact with various biological molecules. This interaction opens avenues for creating innovative diagnostic tools and targeted drug delivery systems. With its favorable properties and broad applicability, this compound stands out as a valuable asset for researchers and industry professionals seeking to advance their projects in organic synthesis and materials development.

Numéro CAS 
127972-00-3
Formule moléculaire
C 8 H 11 BO 3
Poids moléculaire 
165.98
Point de fusion 
97 °C (lit.)
Informations générales
Numéro CAS 
127972-00-3
Formule moléculaire
C 8 H 11 BO 3
Poids moléculaire 
165.98
Point de fusion 
97 °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

2-Methoxy-5-methylphenylboronic 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.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds.
  • Material Science: The compound is applied in the development of advanced materials, including polymers and nanomaterials, enhancing their properties through boron chemistry.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in drug delivery systems.
  • Analytical Chemistry: This boronic acid derivative is utilized in sensor technology for detecting sugars and other biomolecules, providing a sensitive and selective method for analysis.

Citations