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CAS 1150114-68-3

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(5-Chloro-6-ethoxypyridin-3-yl)boronicacid

Description:
(5-Chloro-6-ethoxypyridin-3-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. The compound features a chlorine atom at the 5-position and an ethoxy group at the 6-position of the pyridine, which contributes to its unique chemical properties. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. This compound may exhibit moderate solubility in polar solvents due to the presence of the boronic acid group, while the ethoxy group can enhance its lipophilicity. Its reactivity can be influenced by the electron-withdrawing nature of the chlorine substituent, which can affect the acidity of the boronic acid group. Overall, (5-Chloro-6-ethoxypyridin-3-yl)boronic acid is a versatile compound with potential applications in cross-coupling reactions and as a building block in the synthesis of more complex organic molecules.
Formula:C7H9BClNO3
InChI:InChI=1S/C7H9BClNO3/c1-2-13-7-6(9)3-5(4-10-7)8(11)12/h3-4,11-12H,2H2,1H3
InChI key:InChIKey=PRZRXDHALIHUBT-UHFFFAOYSA-N
SMILES:O(CC)C1=C(Cl)C=C(B(O)O)C=N1
Synonyms:
  • 5-Chloro-6-ethoxypyridine-3-boronic acid
  • Boronic acid, B-(5-chloro-6-ethoxy-3-pyridinyl)-
  • (5-Chloro-6-ethoxypyridin-3-yl)boronicacid
  • (5-Chloro-6-ethoxypyridin-3-yl)boronic acid
  • B-(5-Chloro-6-ethoxy-3-pyridinyl)boronic acid
  • 3-chloro-2-ethoxy-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 5-chloro-6-ethoxypyridin-3-ylboronic&nbsp
  • 5-chloro-6-ethoxypyridin-3-ylboronic acid
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