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CAS 850864-58-3

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B-[5-Chloro-2-(phenylmethoxy)-3-pyridinyl]boronic acid

Description:
B-[5-Chloro-2-(phenylmethoxy)-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 phenylmethoxy 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 molecular architectures. Additionally, the presence of the chlorine atom and the phenylmethoxy group can influence the compound's solubility, stability, and biological activity. Overall, B-[5-Chloro-2-(phenylmethoxy)-3-pyridinyl]boronic acid exemplifies the versatility of boronic acids in synthetic chemistry and their role in drug discovery and development.
Formula:C12H11BClNO3
InChI:InChI=1S/C12H11BClNO3/c14-10-6-11(13(16)17)12(15-7-10)18-8-9-4-2-1-3-5-9/h1-7,16-17H,8H2
InChI key:InChIKey=WSTGGDQWIOLAIE-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(B(O)O)C=C(Cl)C=N2
Synonyms:
  • Boronic acid, [5-chloro-2-(phenylmethoxy)-3-pyridinyl]-
  • Boronic acid, B-[5-chloro-2-(phenylmethoxy)-3-pyridinyl]-
  • [5-Chloro-2-[(phenylmethyl)oxy]-3-pyridinyl]boronic acid
  • B-[5-Chloro-2-(phenylmethoxy)-3-pyridinyl]boronic acid
  • [2-(Benzyloxy)-5-chloropyridin-3-yl]boronic acid
  • 2-(Benzyloxy)-5-chloropyridin-3-ylboronic acid
  • 2-Benzyloxy-5-chloropyridine-3-boronic acid
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