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Catalog Number:
40111
CAS Number:
87199-18-6
3-Hydroxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Hydroxybenzeneboronic acid
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Product Information

3-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 stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique properties allow for applications in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Researchers appreciate its role in the preparation of biologically active compounds, including those targeting cancer and other diseases, due to its ability to enhance the bioavailability of therapeutic agents.

In addition to its synthetic applications, 3-Hydroxyphenylboronic acid is also employed in sensor technology, particularly in the detection of glucose and other biomolecules. This capability is particularly beneficial in the development of diagnostic tools and monitoring devices for diabetes management. The compound's compatibility with various functional groups and its ease of use in laboratory settings make it a preferred choice among chemists and researchers. With its broad range of applications, 3-Hydroxyphenylboronic acid stands out as a valuable asset in both academic and industrial research.

Synonyms
3-Hydroxybenzeneboronic acid
CAS Number
87199-18-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H7BO3
Molecular Weight
137.93
MDL Number
MFCD01074603
PubChem ID
2734359
Melting Point
213 °C (Lit.)
Appearance
White to pale yellow powder
Conditions
Store at RT
General Information
Synonyms
3-Hydroxybenzeneboronic acid
CAS Number
87199-18-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H7BO3
Molecular Weight
137.93
MDL Number
MFCD01074603
PubChem ID
2734359
Melting Point
213 °C (Lit.)
Appearance
White to pale yellow 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-Hydroxyphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in synthesizing pharmaceuticals, particularly in developing targeted therapies for cancer and other diseases due to its ability to form stable complexes with biomolecules.
  • Bioconjugation: It is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems and diagnostic tools.
  • Organic Electronics: The compound is applied in the production of organic semiconductors, which are essential for developing flexible electronic devices, such as OLEDs and solar cells, offering advantages in efficiency and cost.
  • Chemical Sensors: Its properties make it suitable for creating sensors that detect specific biomolecules, providing valuable tools in medical diagnostics and environmental monitoring.
  • Polymer Chemistry: 3-Hydroxyphenylboronic acid is utilized in the synthesis of boron-containing polymers, which have applications in various fields, including materials science and nanotechnology, due to their unique mechanical and thermal properties.

Citations