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CAS 1150114-69-4

:

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

Description:
(5-Chloro-6-isopropoxypyridin-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 substituent at the 5-position and an isopropoxy group at the 6-position of the pyridine, which influences its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in cross-coupling reactions such as Suzuki coupling. This compound may exhibit moderate to high polarity due to the presence of the boronic acid and isopropoxy groups, affecting its solubility in various solvents. Additionally, the chlorine atom can enhance the electrophilicity of the pyridine ring, potentially increasing its reactivity in nucleophilic substitution reactions. Overall, (5-Chloro-6-isopropoxypyridin-3-yl)boronic acid is a versatile building block in medicinal chemistry and materials science, with applications in drug development and the synthesis of complex organic molecules.
Formula:C8H11BClNO3
InChI:InChI=1S/C8H11BClNO3/c1-5(2)14-8-7(10)3-6(4-11-8)9(12)13/h3-5,12-13H,1-2H3
InChI key:InChIKey=LVUBGVPFZYGJSR-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(Cl)C=C(B(O)O)C=N1
Synonyms:
  • 5-Chloro-6-isopropoxypyridine-3-boronic acid
  • Boronic acid, B-[5-chloro-6-(1-methylethoxy)-3-pyridinyl]-
  • B-[5-Chloro-6-(1-methylethoxy)-3-pyridinyl]boronic acid
  • (5-Chloro-6-isopropoxypyridin-3-yl)boronicacid
  • [5-Chloro-6-(propan-2-yloxy)pyridin-3-yl]boronic acid
  • 5-chloro-6-isopropoxypyridin-3-ylboronic&nbsp
  • 5-chloro-6-isopropoxypyridin-3-ylboronic acid
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