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CAS 1451392-07-6

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B-(6-Fluoro-5-methoxy-3-pyridinyl)boronic acid

Description:
B-(6-Fluoro-5-methoxy-3-pyridinyl)boronic acid is a boronic acid derivative characterized by the presence of a pyridine ring substituted with a fluorine atom and a methoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The fluorine substituent can enhance the compound's lipophilicity and influence its biological activity, while the methoxy group may affect its solubility and reactivity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's specific reactivity and interactions can be influenced by its molecular structure, making it a valuable building block in the development of pharmaceuticals and agrochemicals. Overall, B-(6-Fluoro-5-methoxy-3-pyridinyl)boronic acid is a versatile compound with potential applications in various fields of chemistry.
Formula:C6H7BFNO3
InChI:InChI=1S/C6H7BFNO3/c1-12-5-2-4(7(10)11)3-9-6(5)8/h2-3,10-11H,1H3
InChI key:InChIKey=LOTUGWODSACCQG-UHFFFAOYSA-N
SMILES:O(C)C=1C=C(B(O)O)C=NC1F
Synonyms:
  • Boronic acid, B-(6-fluoro-5-methoxy-3-pyridinyl)-
  • B-(6-Fluoro-5-methoxy-3-pyridinyl)boronic acid
  • 2-Fluoro-3-methoxypyridine-5-boronic acid
  • (6-Fluoro-5-methoxypyridin-3-yl)boronicacid
  • 4-Fluoro-5-methoxy-3-pyridinylboronic acid
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