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CAS 1072952-34-1

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(2-Methylpyridin-3-yl)boronic acid hydrochloride (1:1)

Description:
(2-Methylpyridin-3-yl)boronic acid hydrochloride is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydrochloride salt. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The pyridine ring contributes to the compound's aromaticity and can influence its reactivity and interaction with biological systems. Additionally, the hydrochloride form enhances the stability and solubility of the compound, facilitating its use in laboratory settings. Overall, (2-Methylpyridin-3-yl)boronic acid hydrochloride is a valuable reagent in the synthesis of complex organic molecules and in the development of pharmaceuticals.
Formula:C6H9BClNO2
InChI:InChI=1S/C6H8BNO2.ClH/c1-5-6(7(9)10)3-2-4-8-5;/h2-4,9-10H,1H3;1H
SMILES:Cc1c(cccn1)B(O)O.Cl
Synonyms:
  • 2-Methylpyridine-3-boronic acid HCl salt
  • (2-Methylpyridin-3-yl)boronic acid hydrochloride (1:1)
  • 2-METHYLPYRIDIN-3-YLBORONIC ACID HYDROCHLORIDE
  • 2-METHYLPYRIDIN-3-YLBORONIC ACID HCL
  • 2-PICOLINE-3-BORONIC ACID HCL
  • (2-Methyl-3-pyridinyl)boronic acid hydrochloride (1:1)
  • 2-methylpyridin-3-yl-3-boronic acid hydrochloride
  • 2-Methylpyridine-3-boronic acid hydrochloride, 97%
  • 2-Picoline-3-boronic acid hydrochloride
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