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CAS 535934-70-4

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(6-dimethylamino-3-pyridyl)boronic acid dihydrochloride

Description:
(6-Dimethylamino-3-pyridyl)boronic acid dihydrochloride is a boronic acid derivative characterized by its pyridine ring, which contains a dimethylamino group at the 6-position. This compound typically appears as a white to off-white solid and is soluble in water and various organic solvents, making it useful in diverse chemical applications. The presence of the boronic acid functional group allows it to participate in Suzuki-Miyaura cross-coupling reactions, which are vital in organic synthesis for forming carbon-carbon bonds. Additionally, the dihydrochloride form indicates that the compound is protonated, enhancing its solubility and stability in aqueous environments. Its unique structure and reactivity make it valuable in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Safety data should be consulted, as boronic acids can exhibit varying degrees of toxicity and environmental impact. Overall, (6-dimethylamino-3-pyridyl)boronic acid dihydrochloride is a versatile compound with significant implications in both research and industrial applications.
Formula:C8H13BN2O2
InChI:InChI=1/C7H11BN2O2.2ClH/c1-10(2)7-4-3-6(5-9-7)8(11)12;;/h3-5,11-12H,1-2H3;2*1H
SMILES:CN(C)c1ccc(cn1)B(O)O.Cl.Cl
Synonyms:
  • [6-(Dimethylamino)pyridin-3-yl]boronic acid dihydrochloride
  • amino)pyridine-3-boronic acid
  • 6-dimethylamino-4-methyl-pyridineboronic acid
  • 6-(Dimethylamino)-4-methylpyridine-3-boronic acid
  • (6-Dimethylamino-4-methyl-3-pyridinyl)boronic acid
  • 2-dimethylamino-4-methyl-5-pyridyl boronic acid
  • Boronic acid, B-[6-(dimethylamino)-4-methyl-3-pyridinyl]-
  • 2-(Dimethylamino)-4-methylpyridine-5-boronic acid
  • 6-(diMethylaMino)-4-Methylpyridin-3-ylboronic acid
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