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CAS 913835-99-1

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5-(tert-Butylcarbamoyl)pyridine-3-boronic acid

Description:
5-(tert-Butylcarbamoyl)pyridine-3-boronic acid is a chemical compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a pyridine ring, which contributes to its aromatic properties and potential biological activity. The tert-butylcarbamoyl group enhances its solubility and stability, while also influencing its reactivity. This compound is typically used in the development of pharmaceuticals and agrochemicals, particularly in the synthesis of complex organic molecules. Its boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Additionally, the presence of the pyridine ring may impart specific electronic properties, making it a candidate for various chemical transformations. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C10H15BN2O3
InChI:InChI=1/C10H15BN2O3/c1-10(2,3)13-9(14)7-4-8(11(15)16)6-12-5-7/h4-6,15-16H,1-3H3,(H,13,14)
SMILES:CC(C)(C)N=C(c1cc(cnc1)B(O)O)O
Synonyms:
  • [5-(tert-Butylcarbamoyl)pyridin-3-yl]boronic acid
  • boronic acid, B-[5-[[(1,1-dimethylethyl)amino]carbonyl]-3-pyridinyl]-
  • [5-(Tert-Butylcarbamoyl)-3-Pyridyl]Boronic Acid
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