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CAS 2096341-73-8

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B-[4-Chloro-3-(3-pyridinylmethoxy)phenyl]boronic acid

Description:
B-[4-Chloro-3-(3-pyridinylmethoxy)phenyl]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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a chlorine atom and a pyridinylmethoxy group, contributing to its potential biological activity and interaction with specific targets. The boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the pyridine ring may enhance the compound's solubility and reactivity, making it suitable for various chemical transformations. Its unique structure suggests potential applications in drug development, particularly in the design of inhibitors for specific enzymes or receptors. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and the need for proper storage conditions to maintain stability.
Formula:C12H11BClNO3
InChI:InChI=1S/C12H11BClNO3/c14-11-4-3-10(13(16)17)6-12(11)18-8-9-2-1-5-15-7-9/h1-7,16-17H,8H2
InChI key:InChIKey=FIYZIBCQFDRMGC-UHFFFAOYSA-N
SMILES:O(CC=1C=CC=NC1)C2=CC(B(O)O)=CC=C2Cl
Synonyms:
  • Boronic acid, B-[4-chloro-3-(3-pyridinylmethoxy)phenyl]-
  • B-[4-Chloro-3-(3-pyridinylmethoxy)phenyl]boronic acid
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