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Catalog Number:
24576
CAS Number:
25487-66-5
3-Carboxyphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
3-(Dihydroxyboronyl)benzoic acid
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Product Information

3-Carboxyphenylboronic acid is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative features a carboxylic acid group that enhances its reactivity, making it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique ability to form reversible covalent bonds with diols allows for the creation of complex molecular architectures, which is particularly valuable in the synthesis of biologically active compounds. Researchers utilize 3-Carboxyphenylboronic acid in the development of targeted drug delivery systems and in the design of sensors for glucose monitoring, showcasing its relevance in both health and environmental applications.

Additionally, this compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in the synthesis of advanced materials and fine chemicals. Its stability and ease of handling make it a preferred choice for chemists looking to streamline their synthetic processes. With its diverse applications and significant role in modern chemistry, 3-Carboxyphenylboronic acid stands out as a valuable asset for researchers and industry professionals alike.

Synonyms
3-(Dihydroxyboronyl)benzoic acid
CAS Number
25487-66-5
Purity
≥ 98% (HPLC)
Molecular Formula
C7H7BO4
Molecular Weight
165.94
MDL Number
MFCD00036833
PubChem ID
2733957
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
3-(Dihydroxyboronyl)benzoic acid
CAS Number
25487-66-5
Purity
≥ 98% (HPLC)
Molecular Formula
C7H7BO4
Molecular Weight
165.94
MDL Number
MFCD00036833
PubChem ID
2733957
Appearance
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

3-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 anti-cancer agents. Its ability to form reversible covalent bonds with biomolecules enhances drug efficacy.
  • Bioconjugation: It is commonly used in bioconjugation techniques to attach biomolecules like proteins and antibodies to surfaces or other molecules, facilitating targeted drug delivery systems.
  • Organic Electronics: In the field of organic electronics, this compound is employed in the fabrication of organic semiconductors, improving the performance of devices like organic light-emitting diodes (OLEDs) and solar cells.
  • Sensor Development: 3-Carboxyphenylboronic acid is utilized in the creation of chemical sensors for glucose detection, offering a practical solution for diabetes management through real-time monitoring.
  • Polymer Chemistry: It plays a significant role in the development of functional polymers, enhancing properties such as thermal stability and mechanical strength, which are crucial for various industrial applications.

Citations