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CAS 1451391-01-7

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B-[2-Fluoro-5-(1-methylethoxy)-3-pyridinyl]boronic acid

Description:
B-[2-Fluoro-5-(1-methylethoxy)-3-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling. The compound features a pyridine ring substituted with a fluorine atom and an isopropoxy group, which can influence its reactivity and solubility. The fluorine substitution can enhance the electronic properties of the pyridine, potentially affecting its interaction with biological targets or other chemical species. Boronic acids are often utilized in medicinal chemistry and materials science due to their ability to participate in cross-coupling reactions and their role in the development of sensors and drug delivery systems. The specific structure of this compound suggests potential applications in pharmaceutical research, particularly in the development of targeted therapies or as intermediates in organic synthesis. Its unique characteristics stem from the combination of the boronic acid functionality and the substituted pyridine ring, which together contribute to its chemical behavior and reactivity.
Formula:C8H11BFNO3
InChI:InChI=1S/C8H11BFNO3/c1-5(2)14-6-3-7(9(12)13)8(10)11-4-6/h3-5,12-13H,1-2H3
InChI key:InChIKey=RFZYRXLTARRVRZ-UHFFFAOYSA-N
SMILES:O(C(C)C)C=1C=C(B(O)O)C(F)=NC1
Synonyms:
  • B-[2-Fluoro-5-(1-methylethoxy)-3-pyridinyl]boronic acid
  • Boronic acid, B-[2-fluoro-5-(1-methylethoxy)-3-pyridinyl]-
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