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Catalog Number:
28818
CAS Number:
174669-73-9
2-Fluoropyridine-3-boronic acid
Purity:
≥ 98% (Assay)
Documents
$18.53 /1G
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Product Information

2-Fluoropyridine-3-boronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of complex organic molecules. Its unique fluorine substituent enhances its reactivity and selectivity, allowing researchers to develop novel pharmaceuticals and agrochemicals with improved efficacy.

In addition to its synthetic applications, 2-Fluoropyridine-3-boronic acid has shown promise in the development of targeted therapies, particularly in the field of cancer research. Its ability to form stable complexes with various substrates makes it a valuable tool for scientists aiming to explore new pathways in drug discovery. With its favorable properties and broad applicability, this compound is an excellent choice for researchers seeking to innovate in the fields of chemistry and pharmaceuticals.

CAS Number
174669-73-9
Purity
≥ 98% (Assay)
Molecular Formula
C5H5BFNO2
Molecular Weight
140.91
MDL Number
MFCD03411557
PubChem ID
2783270
Appearance
Off-white powder
Conditions
Store at 0-8°C
General Information
CAS Number
174669-73-9
Purity
≥ 98% (Assay)
Molecular Formula
C5H5BFNO2
Molecular Weight
140.91
MDL Number
MFCD03411557
PubChem ID
2783270
Appearance
Off-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

2-Fluoropyridine-3-boronic 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 therapies for cancer and other diseases.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create complex organic molecules, making it invaluable for chemists in the field of organic synthesis.
  • Material Science: The compound is used in the production of advanced materials, including polymers and coatings, that require specific chemical properties for enhanced performance.
  • Agricultural Chemistry: It plays a role in the development of agrochemicals, contributing to the formulation of herbicides and pesticides that are more effective and environmentally friendly.
  • Analytical Chemistry: This chemical is utilized in various analytical techniques, aiding researchers in the detection and quantification of other compounds in complex mixtures.

Citations