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Catalog Number:
40337
CAS Number:
246023-54-1
Acide 4-méthoxy-2,5-diméthylphénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-méthoxy-2,5-diméthylbenzèneboronique
Documents
$115.27 /1G
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Informations sur le produit

4-Methoxy-2,5-dimethylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a methoxy group and two methyl substituents, enhances its reactivity and selectivity, allowing for the efficient formation of carbon-carbon bonds. Researchers appreciate its role in developing novel compounds with potential therapeutic applications, particularly in the field of cancer research and drug discovery.

In addition to its synthetic utility, 4-Methoxy-2,5-dimethylphenylboronic acid exhibits favorable solubility characteristics, which facilitate its use in various reaction conditions. Its compatibility with a range of functional groups makes it an attractive choice for chemists looking to streamline their synthetic pathways. With its proven efficacy in diverse applications, this compound stands out as a valuable resource for professionals seeking to innovate in organic synthesis and medicinal chemistry.

Numéro CAS 
246023-54-1
Formule moléculaire
C 9 H 13 BO 3
Poids moléculaire 
180.01
Informations générales
Numéro CAS 
246023-54-1
Formule moléculaire
C 9 H 13 BO 3
Poids moléculaire 
180.01
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-Methoxy-2,5-dimethylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate 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 cross-coupling reactions, allowing researchers to create complex carbon-carbon bonds efficiently, which is essential in drug discovery.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation processes for labeling biomolecules in diagnostics and therapeutic applications.
  • Material Science: This compound is applied in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and mechanical strength.
  • Sensor Development: Its ability to interact with specific biomolecules makes it valuable in creating sensors for detecting glucose and other metabolites, beneficial in medical diagnostics.

Citations