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Catalog Number:
40166
CAS Number:
182344-25-8
4-Fluoro-1-naphthaleneboronic acid
Purity:
≥ 98% (HPLC)
Documents
$22.43 /200MG
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Product Information

4-Fluoro-1-naphthaleneboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a fluorine substituent that enhances its reactivity and selectivity in various chemical reactions, making it an invaluable tool for researchers. Its unique structure allows for the formation of stable complexes with diols, which is particularly beneficial in the development of pharmaceutical intermediates and in the synthesis of biologically active compounds.

In addition to its applications in drug discovery, 4-Fluoro-1-naphthaleneboronic acid is also employed in materials science, particularly in the development of organic electronics and sensors. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it a key component in the synthesis of complex organic molecules, facilitating advancements in both academic research and industrial applications. With its favorable properties and broad applicability, this compound is essential for professionals seeking to innovate in the fields of chemistry and materials science.

CAS Number
182344-25-8
Purity
≥ 98% (HPLC)
Molecular Formula
C10H8BFO2
Molecular Weight
189.98
MDL Number
MFCD04039221
PubChem ID
2782675
Melting Point
240 - 244 °C
Appearance
White to orange crystalline powder
Conditions
Store at RT
General Information
CAS Number
182344-25-8
Purity
≥ 98% (HPLC)
Molecular Formula
C10H8BFO2
Molecular Weight
189.98
MDL Number
MFCD04039221
PubChem ID
2782675
Melting Point
240 - 244 °C
Appearance
White to orange crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Fluoro-1-naphthaleneboronic 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 in the development of targeted cancer therapies due to its ability to form stable complexes with biomolecules.
  • Organic Synthesis: It is employed in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic molecules. This application is particularly valuable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the creation of advanced materials, including organic semiconductors and sensors, enhancing the performance of electronic devices.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for developing diagnostic tools and therapeutic agents.
  • Environmental Monitoring: This chemical can be utilized in the detection and analysis of environmental pollutants, contributing to efforts in environmental protection and sustainability.

Citations