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CAS 1150114-70-7

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B-(5-Chloro-6-propoxy-3-pyridinyl)boronic acid

Description:
B-(5-Chloro-6-propoxy-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 and other nucleophiles. This compound features a pyridine ring substituted with a chlorine atom and a propoxy group, contributing to its unique chemical reactivity and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis for constructing complex molecules. Additionally, the presence of the chlorine and propoxy substituents can influence the compound's solubility, stability, and biological activity. Its specific properties, such as melting point, solubility, and reactivity, would depend on the molecular interactions and the environment in which it is used. Overall, B-(5-Chloro-6-propoxy-3-pyridinyl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C8H11BClNO3
InChI:InChI=1S/C8H11BClNO3/c1-2-3-14-8-7(10)4-6(5-11-8)9(12)13/h4-5,12-13H,2-3H2,1H3
InChI key:InChIKey=RJBPIJZCHZZPHC-UHFFFAOYSA-N
SMILES:O(CCC)C1=C(Cl)C=C(B(O)O)C=N1
Synonyms:
  • B-(5-Chloro-6-propoxy-3-pyridinyl)boronic acid
  • Boronic acid, B-(5-chloro-6-propoxy-3-pyridinyl)-
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