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CAS 1029654-18-9

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

Description:
B-(2,5-Dimethyl-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has two methyl substituents at the 2 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 presence of the pyridine ring contributes to its aromatic character and potential for coordination with metal ions. Additionally, the methyl groups can influence the compound's solubility and reactivity. B-(2,5-Dimethyl-3-pyridinyl)boronic acid is often utilized in cross-coupling reactions, particularly in the Suzuki-Miyaura reaction, which is a key method for forming carbon-carbon bonds in organic synthesis. Its unique structure and functional properties make it a valuable building block in the development of pharmaceuticals and agrochemicals.
Formula:C7H10BNO2
InChI:InChI=1S/C7H10BNO2/c1-5-3-7(8(10)11)6(2)9-4-5/h3-4,10-11H,1-2H3
InChI key:InChIKey=HIMKPXQJBGSLSM-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)N=CC(C)=C1
Synonyms:
  • 2,5-Dimethylpyridin-3-ylboronic acid
  • 2,5-Dimethylpyridine-3-boronic acid
  • B-(2,5-Dimethyl-3-pyridinyl)boronic acid
  • Boronic acid, B-(2,5-dimethyl-3-pyridinyl)-
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