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CAS 1072951-54-2

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B-(2,6-Dichloro-4-pyridinyl)boronic acid

Description:
B-(2,6-Dichloro-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that is substituted with two chlorine atoms at the 2 and 6 positions. This compound typically exhibits properties such as being a white to off-white solid, and it is soluble in polar solvents like water and methanol, which is a common trait for boronic acids due to their ability to form hydrogen bonds. The presence of the boronic acid group allows it to participate in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Additionally, the chlorinated pyridine moiety can enhance the compound's reactivity and biological activity. Its unique structure may also contribute to specific interactions with biological targets, making it of interest in pharmaceutical research. As with many boronic acids, it may exhibit sensitivity to moisture and should be handled with care to maintain its stability and reactivity.
Formula:C5H4BCl2NO2
InChI:InChI=1S/C5H4BCl2NO2/c7-4-1-3(6(10)11)2-5(8)9-4/h1-2,10-11H
InChI key:InChIKey=JFUQZFQJFYZZGY-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(Cl)N=C(Cl)C1
Synonyms:
  • 2,6-Dichloropyridine-4-boronic acid
  • 2,6-Dichloropyridine-4-boronicacid
  • B-(2,6-Dichloro-4-pyridinyl)boronic acid
  • Boronic acid, B-(2,6-dichloro-4-pyridinyl)-
  • 2,6-Dichloropyridin-4-ylboronic acid
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