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Catalog Number:
40279
CAS Number:
182344-14-5
Acide 3-fluoro-4-hydroxyphénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-fluoro-4-hydroxybenzèneboronique
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Product Information

3-Fluoro-4-hydroxyphenylboronic acid is a versatile compound widely utilized in pharmaceutical and chemical research. Known for its unique boronic acid functionality, this compound serves as a crucial building block in the synthesis of various biologically active molecules. Its ability to form reversible covalent bonds with diols makes it particularly valuable in the development of targeted drug delivery systems and in the design of sensors for glucose monitoring. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic frameworks in medicinal chemistry.

In addition to its applications in organic synthesis, 3-Fluoro-4-hydroxyphenylboronic acid is recognized for its potential in materials science, particularly in the development of advanced polymers and nanomaterials. Its unique properties enable the creation of functional materials with tailored characteristics, making it a sought-after compound for innovative research. With its broad range of applications and significant advantages over similar compounds, this boronic acid derivative is an essential tool for scientists and industry professionals aiming to push the boundaries of chemical research and development.

Synonyms
Acide 3-fluoro-4-hydroxybenzèneboronique
CAS Number
182344-14-5
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C 6 H 6 BFO 3
Molecular Weight
155.92
MDL Number
MFCD06659838
PubChem ID
23005361
Melting Point
256 °C (lit.)
Appearance
Poudre cristalline blanche à légèrement jaune
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-fluoro-4-hydroxybenzèneboronique
CAS Number
182344-14-5
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C 6 H 6 BFO 3
Molecular Weight
155.92
MDL Number
MFCD06659838
PubChem ID
23005361
Melting Point
256 °C (lit.)
Appearance
Poudre cristalline blanche à légèrement jaune
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-Fluoro-4-hydroxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly those targeting cancer and other diseases. Its unique properties enhance the efficacy of drug candidates.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules. This application is vital in creating targeted drug delivery systems.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, which can exhibit enhanced mechanical and thermal properties.
  • Analytical Chemistry: It plays a role in analytical methods, such as chromatography and spectroscopy, where it aids in the detection and quantification of various analytes due to its reactivity with specific functional groups.
  • Environmental Science: This chemical is also investigated for its potential in environmental applications, such as the removal of pollutants from water, showcasing its versatility beyond traditional uses.

Citations