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CAS 1218790-95-4

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B-[2-(2-Methylpropoxy)-3-pyridinyl]boronic acid

Description:
B-[2-(2-Methylpropoxy)-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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a pyridine ring, which contributes to its aromatic properties and potential biological activity. The presence of the 2-methylpropoxy group enhances its solubility and may influence its reactivity and interaction with biological targets. This compound is typically a white to off-white solid and is soluble in polar organic solvents. Its boronic acid functionality allows it to participate in cross-coupling reactions, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals. Additionally, boronic acids can act as enzyme inhibitors, which may have implications in medicinal chemistry. Overall, B-[2-(2-Methylpropoxy)-3-pyridinyl]boronic acid is a versatile compound with significant applications in organic synthesis and potential therapeutic uses.
Formula:C9H14BNO3
InChI:InChI=1S/C9H14BNO3/c1-7(2)6-14-9-8(10(12)13)4-3-5-11-9/h3-5,7,12-13H,6H2,1-2H3
InChI key:InChIKey=VMPOWUYMVMJUSI-UHFFFAOYSA-N
SMILES:O(CC(C)C)C1=C(B(O)O)C=CC=N1
Synonyms:
  • 2-Isobutoxypyridine-3-boronic acid
  • (2-Isobutoxypyridin-3-yl)boronic acid
  • Boronic acid, B-[2-(2-methylpropoxy)-3-pyridinyl]-
  • B-[2-(2-Methylpropoxy)-3-pyridinyl]boronic acid
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