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CAS 1072952-39-6

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B-(2-Chloro-3-fluoro-5-methyl-4-pyridinyl)boronic acid

Description:
B-(2-Chloro-3-fluoro-5-methyl-4-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 chlorine atom and a fluorine atom at the 2 and 3 positions, respectively, along with a methyl group at the 5 position of the pyridine ring, contributing to its unique reactivity and properties. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents can enhance the compound's reactivity and influence its interactions with biological targets. Additionally, the compound may exhibit specific solubility characteristics in polar solvents due to the boronic acid group, which can also participate in hydrogen bonding. Overall, B-(2-Chloro-3-fluoro-5-methyl-4-pyridinyl)boronic acid is a versatile compound with potential applications in drug development and materials science.
Formula:C6H6BClFNO2
InChI:InChI=1S/C6H6BClFNO2/c1-3-2-10-6(8)5(9)4(3)7(11)12/h2,11-12H,1H3
InChI key:InChIKey=NJMMLPABMFWKGC-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(F)=C(Cl)N=CC1C
Synonyms:
  • Boronic acid, B-(2-chloro-3-fluoro-5-methyl-4-pyridinyl)-
  • B-(2-Chloro-3-fluoro-5-methyl-4-pyridinyl)boronic acid
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