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Catalog Number:
40210
CAS Number:
175883-60-0
Acide 3-chloro-4-méthoxyphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-chloro-4-méthoxybenzèneboronique
Documents
$42.46 /1G
Taille
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Informations sur le produit

3-Chloro-4-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a chloro and methoxy group, enhances its reactivity and selectivity, allowing researchers to create targeted compounds with improved efficacy and reduced side effects.

In addition to its applications in drug development, 3-Chloro-4-methoxyphenylboronic acid is also employed in the production of advanced materials and polymers. Its compatibility with various functional groups enables chemists to explore innovative pathways in material science, leading to the development of new technologies. With its proven track record in enhancing synthetic efficiency and product specificity, this compound stands out as a valuable asset for researchers and industry professionals seeking to push the boundaries of chemical innovation.

Numéro CAS 
175883-60-0
Formule moléculaire
C7H8BClO3
Poids moléculaire 
186.4
Point de fusion 
242 °C (lit.)
Informations générales
Numéro CAS 
175883-60-0
Formule moléculaire
C7H8BClO3
Poids moléculaire 
186.4
Point de fusion 
242 °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-Chloro-4-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, due to its ability to form stable complexes with biomolecules.
  • Organic Synthesis: It is employed in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently, which is essential in materials science and drug discovery.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, enhancing the specificity of assays in biochemical research.
  • Sensor Technology: This compound is utilized in developing chemical sensors for detecting glucose levels, providing a practical application in diabetes management through real-time monitoring.
  • Environmental Chemistry: It is also researched for its potential in environmental applications, such as the removal of pollutants from water, showcasing its versatility beyond traditional chemical applications.

Citations