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CAS 870521-30-5

:

B-[6-(1-Methylethoxy)-3-pyridinyl]boronic acid

Description:
B-[6-(1-Methylethoxy)-3-pyridinyl]boronic acid, with the CAS number 870521-30-5, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically exhibits properties such as moderate solubility in polar organic solvents and water, owing to the presence of the boronic acid moiety, which can engage in hydrogen bonding. The methylethoxy substituent enhances its lipophilicity, potentially influencing its biological activity and reactivity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including medicinal chemistry and materials science. This specific compound may be utilized in the development of pharmaceuticals, particularly in the context of targeted therapies, due to its ability to interact with biological molecules. Additionally, its structural features suggest potential applications in organic synthesis and catalysis, where boron-containing compounds play a crucial role in facilitating chemical transformations.
Formula:C8H12BNO3
InChI:InChI=1S/C8H12BNO3/c1-6(2)13-8-4-3-7(5-10-8)9(11)12/h3-6,11-12H,1-2H3
InChI key:InChIKey=SGEOBUJTURUUJE-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=CC=C(B(O)O)C=N1
Synonyms:
  • (6-Isopropoxy-3-pyridyl)boronic acid
  • (6-Propan-2-yloxypyridin-3-yl)boronic acid
  • 2-Isopropoxypyridine-5-boronic acid
  • 6-Isopropoxypyridin-3-Ylboronic Acid
  • 6-Isopropoxypyridine-3-boronic acid
  • B-[6-(1-Methylethoxy)-3-pyridinyl]boronic acid
  • Boronic acid, B-[6-(1-methylethoxy)-3-pyridinyl]-
  • Boronic acid, [6-(1-methylethoxy)-3-pyridinyl]-
  • (6-Isopropoxypyridin-3-yl)boronic acid
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