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Catalog Number:
40322
CAS Number:
136496-72-5
Acide 4-carboxy-3-chlorophénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-carboxy-3-chlorobenzèneboronique
Documents
$145.52 /1G
Taille
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Informations sur le produit

4-Carboxy-3-chlorophenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique properties allow it to serve as a key building block in the synthesis of biologically active compounds, particularly in the creation of targeted therapies for cancer and other diseases. Researchers appreciate its role in Suzuki coupling reactions, which are crucial for constructing complex organic molecules with precision.

In addition to its applications in drug development, 4-Carboxy-3-chlorophenylboronic acid is also valuable in materials science, particularly in the design of sensors and polymers. Its ability to interact with different functional groups enhances its utility in creating innovative materials with tailored properties. The compound's stability and reactivity make it a preferred choice for researchers looking to streamline their synthesis processes while achieving high yields. With its broad range of applications, this compound stands out as a significant tool for professionals in both the pharmaceutical and materials industries.

Numéro CAS 
136496-72-5
Formule moléculaire
C7H6BClO4
Poids moléculaire 
200.38
Point de fusion 
232 °C (déc.)
Informations générales
Numéro CAS 
136496-72-5
Formule moléculaire
C7H6BClO4
Poids moléculaire 
200.38
Point de fusion 
232 °C (déc.)
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-Carboxy-3-chlorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting cancer and diabetes, due to its ability to form stable complexes with biomolecules.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach drugs or imaging agents to proteins, enhancing their therapeutic efficacy and diagnostic capabilities.
  • Material Science: The compound is used in the development of advanced materials, such as sensors and polymers, where its boronic acid functionality can form dynamic covalent bonds, leading to innovative applications in electronics.
  • Organic Synthesis: It plays a significant role in organic synthesis as a reagent for Suzuki-Miyaura coupling reactions, which are vital for constructing complex organic molecules in a more efficient manner.
  • Environmental Monitoring: This chemical is also applied in environmental science for detecting and quantifying phenolic compounds in water samples, contributing to pollution control and environmental safety.

Citations