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Catalog Number:
40315
CAS Number:
219735-99-6
Acide 2-chloro-4-méthoxyphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-chloro-4-méthoxybenzèneboronique
Documents
$52.68 /1G
Taille
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Informations sur le produit

2-Chloro-4-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to develop pharmaceuticals, agrochemicals, and advanced materials. Its effectiveness in facilitating the formation of carbon-carbon bonds enhances the synthesis of complex organic molecules, thereby streamlining the development of innovative compounds.

Additionally, 2-Chloro-4-methoxyphenylboronic acid serves as a valuable building block in the synthesis of biologically active compounds, including potential drug candidates. Its favorable reactivity profile and compatibility with various functional groups allow for diverse applications in chemical research and development. With its proven track record in enhancing synthetic efficiency, this compound is an indispensable tool for chemists aiming to push the boundaries of modern chemistry.

Numéro CAS 
219735-99-6
Formule moléculaire
C7H8BClO3
Poids moléculaire 
186.4
Point de fusion 
202 °C (lit.)
Informations générales
Numéro CAS 
219735-99-6
Formule moléculaire
C7H8BClO3
Poids moléculaire 
186.4
Point de fusion 
202 °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-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, enhancing drug efficacy and specificity.
  • Organic Synthesis: It is employed in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently, which is crucial for developing new materials and chemicals.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation techniques for creating targeted drug delivery systems.
  • Material Science: This compound is used in the production of boron-containing polymers, which exhibit unique properties such as enhanced thermal stability and electrical conductivity, beneficial for electronic applications.
  • Analytical Chemistry: It acts as a reagent in various analytical methods, including chromatography and mass spectrometry, aiding in the detection and quantification of biomolecules.

Citations