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Catalog Number:
40238
CAS Number:
913835-32-2
3-Carboxy-4-chlorophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-Carboxy-4-chlorobenzeneboronic acid
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Product Information

3-Carboxy-4-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 pharmaceutical agents and agrochemicals. Its unique structure allows for selective reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Researchers appreciate its role in the synthesis of biologically active compounds, including potential anti-cancer agents and other therapeutic drugs.

In addition to its synthetic applications, 3-Carboxy-4-chlorophenylboronic acid has shown promise in materials science, particularly in the development of sensors and advanced materials due to its ability to interact with specific biomolecules. This compound's stability and reactivity make it a valuable tool for chemists looking to innovate in drug discovery and materials engineering. Its practical applications, combined with its unique properties, position it as a key player in both research and industrial settings.

Synonyms
3-Carboxy-4-chlorobenzeneboronic acid
CAS Number
913835-32-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H6BClO4
Molecular Weight
200.38
MDL Number
MFCD06801689
PubChem ID
23005333
Melting Point
225 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Carboxy-4-chlorobenzeneboronic acid
CAS Number
913835-32-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H6BClO4
Molecular Weight
200.38
MDL Number
MFCD06801689
PubChem ID
23005333
Melting Point
225 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Carboxy-4-chlorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in synthesizing various pharmaceuticals, particularly in the development of anti-cancer agents. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, allowing researchers to create complex molecules through Suzuki coupling reactions, which are essential in producing fine chemicals and agrochemicals.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules for targeted drug delivery systems. This application is vital in improving the specificity and effectiveness of therapeutic agents.
  • Sensor Technology: Its properties make it suitable for developing sensors that detect specific biomolecules, aiding in diagnostics and environmental monitoring, which is crucial for healthcare and safety applications.
  • Material Science: The compound is also explored in creating advanced materials, such as polymers with enhanced properties, which can be applied in various industries, including electronics and packaging.

Citations