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CAS 1309982-33-9

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B-(3,5-Dichloro-2-pyridinyl)boronic acid

Description:
B-(3,5-Dichloro-2-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 3 and 5 positions. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The dichloropyridine moiety contributes to its reactivity and potential biological activity, as halogenated pyridines can influence the compound's interaction with biological targets. Additionally, the presence of the boron atom allows for participation in cross-coupling reactions, which are essential in the formation of carbon-carbon bonds in synthetic organic chemistry. Overall, B-(3,5-Dichloro-2-pyridinyl)boronic acid is a versatile compound with significant utility in both research and industrial applications.
Formula:C5H4BCl2NO2
InChI:InChI=1S/C5H4BCl2NO2/c7-3-1-4(8)5(6(10)11)9-2-3/h1-2,10-11H
InChI key:InChIKey=CCCOOLMYLSYCLX-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=C(Cl)C=N1
Synonyms:
  • Boronic acid, B-(3,5-dichloro-2-pyridinyl)-
  • B-(3,5-Dichloro-2-pyridinyl)boronic acid
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