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Catalog Number:
31431
CAS Number:
71597-85-8
4-Hydroxyphenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
4-Hydroxybenzeneboronic acid, p-Hydroxyphenylboronic acid
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Product Information

4-Hydroxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form reversible covalent bonds with diols, making it an essential reagent in the development of various pharmaceutical agents and materials. Its unique properties enable it to act as a key building block in the synthesis of complex organic molecules, particularly in the preparation of biologically active compounds. Researchers have effectively employed 4-Hydroxyphenylboronic acid in the development of targeted drug delivery systems and in the synthesis of fluorescent probes for biological imaging, showcasing its significant potential in both academic and industrial applications.

Additionally, this compound is valuable in the field of materials science, where it is used in the fabrication of advanced polymers and hydrogels. Its ability to enhance the mechanical properties of materials while maintaining biocompatibility makes it an attractive choice for biomedical applications. With its broad range of applications and unique reactivity, 4-Hydroxyphenylboronic acid stands out as a crucial tool for researchers and industry professionals looking to innovate and improve their chemical processes.

Synonyms
4-Hydroxybenzeneboronic acid, p-Hydroxyphenylboronic acid
CAS Number
71597-85-8
Purity
≥ 99% (HPLC)
Molecular Formula
C6H7BO3
Molecular Weight
137.93
MDL Number
MFCD01074628
PubChem ID
2734360
Melting Point
> 230 ?C
Appearance
Hazel powder
Conditions
Store at RT
General Information
Synonyms
4-Hydroxybenzeneboronic acid, p-Hydroxyphenylboronic acid
CAS Number
71597-85-8
Purity
≥ 99% (HPLC)
Molecular Formula
C6H7BO3
Molecular Weight
137.93
MDL Number
MFCD01074628
PubChem ID
2734360
Melting Point
> 230 ?C
Appearance
Hazel 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

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

  • Drug Development: This compound is used in the synthesis of boron-containing pharmaceuticals, enhancing drug efficacy and targeting specific biological pathways.
  • Bioconjugation: It serves as a key reagent for attaching biomolecules, such as proteins and nucleic acids, to surfaces or other molecules, facilitating advanced diagnostic and therapeutic applications.
  • Organic Synthesis: The compound plays a crucial role in cross-coupling reactions, which are essential for creating complex organic molecules in the chemical industry.
  • Sensor Technology: Its properties allow for the development of sensors that detect glucose levels, making it valuable in diabetes management and research.
  • Material Science: 4-Hydroxyphenylboronic acid is used to modify polymers, improving their properties for applications in coatings, adhesives, and electronics.

Citations