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CAS 1217501-42-2

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

Description:
B-[5-Chloro-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 and other nucleophiles. This compound features a pyridine ring substituted with a chlorine atom and a branched alkoxy group, specifically a 2-methylpropoxy group, which contributes to its solubility and reactivity. The boronic acid moiety is significant in various applications, particularly in organic synthesis and medicinal chemistry, where it can serve as a key intermediate in the development of pharmaceuticals. Additionally, compounds like this one are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for forming carbon-carbon bonds. The presence of the chlorine substituent may influence the electronic properties and reactivity of the molecule, making it a valuable candidate for further research in drug development and material science. Overall, this compound exemplifies the versatility and importance of boronic acids in modern chemistry.
Formula:C9H13BClNO3
InChI:InChI=1S/C9H13BClNO3/c1-6(2)5-15-9-8(10(13)14)3-7(11)4-12-9/h3-4,6,13-14H,5H2,1-2H3
InChI key:InChIKey=RMJKPMVBIIUTRL-UHFFFAOYSA-N
SMILES:O(CC(C)C)C1=C(B(O)O)C=C(Cl)C=N1
Synonyms:
  • B-[5-Chloro-2-(2-methylpropoxy)-3-pyridinyl]boronic acid
  • Boronic acid, B-[5-chloro-2-(2-methylpropoxy)-3-pyridinyl]-
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