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Catalog Number:
28086
CAS Number:
14047-29-1
4-Carboxyphenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
p-Carboxyphenylboronic acid
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Product Information

4-Carboxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and materials science. This boronic acid derivative features a carboxylic acid group, making it an excellent candidate for various applications, including drug discovery and development, where it serves as a crucial building block for the synthesis of biologically active molecules. Its ability to form reversible covalent bonds with diols enhances its utility in the design of sensors and as a reagent in cross-coupling reactions, particularly in the Suzuki-Miyaura coupling process, which is essential for constructing complex organic frameworks.

Additionally, 4-Carboxyphenylboronic acid is recognized for its role in the development of polymeric materials and nanocomposites, where it can improve mechanical properties and thermal stability. Researchers appreciate its compatibility with a range of functional groups, allowing for diverse modifications and applications in fields such as medicinal chemistry, materials science, and environmental chemistry. This compound stands out for its unique ability to facilitate the formation of stable complexes with carbohydrates, making it valuable in biosensor applications and carbohydrate recognition studies.

Synonyms
p-Carboxyphenylboronic acid
CAS Number
14047-29-1
Purity
≥ 99% (HPLC)
Molecular Formula
C7H7BO4
Molecular Weight
165.94
MDL Number
MFCD00151801
PubChem ID
312183
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
p-Carboxyphenylboronic acid
CAS Number
14047-29-1
Purity
≥ 99% (HPLC)
Molecular Formula
C7H7BO4
Molecular Weight
165.94
MDL Number
MFCD00151801
PubChem ID
312183
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Carboxyphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules, enhancing the specificity and efficacy of drug delivery systems.
  • Sensor Technology: The compound is employed in the fabrication of sensors for detecting glucose and other biomolecules, making it valuable in diabetes management and biosensing applications.
  • Material Science: It plays a role in creating advanced materials, such as polymers and nanocomposites, which are used in electronics and packaging industries.
  • Chemical Synthesis: This chemical is a versatile reagent in organic synthesis, facilitating the formation of complex molecules, which is essential in various research and industrial applications.

Citations