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CAS 1072944-22-9

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B-(6-Bromo-2-methyl-3-pyridinyl)boronic acid

Description:
B-(6-Bromo-2-methyl-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a bromine atom at the 6-position and a methyl group at the 2-position of the pyridine, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various chemical reactions, including Suzuki coupling, which is a method for forming carbon-carbon bonds. The presence of the bromine substituent enhances its electrophilic character, facilitating further functionalization. Additionally, the compound may exhibit interesting biological properties, making it a candidate for drug development or as a tool in chemical biology. Its solubility and stability in various solvents can vary, influencing its practical applications in laboratory settings. Overall, B-(6-Bromo-2-methyl-3-pyridinyl)boronic acid is a versatile compound with significant implications in synthetic and medicinal chemistry.
Formula:C6H7BBrNO2
InChI:InChI=1S/C6H7BBrNO2/c1-4-5(7(10)11)2-3-6(8)9-4/h2-3,10-11H,1H3
InChI key:InChIKey=NXLYPZNXELJJDT-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)N=C(Br)C=C1
Synonyms:
  • Boronic acid, B-(6-bromo-2-methyl-3-pyridinyl)-
  • B-(6-Bromo-2-methyl-3-pyridinyl)boronic acid
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