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CAS 1028749-31-6

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6-(cyclopropylmethoxy)pyridine-3-boronic acid

Description:
6-(Cyclopropylmethoxy)pyridine-3-boronic acid is an organic 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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a pyridine ring, which contributes to its aromatic properties and potential for coordination with metal catalysts. The cyclopropylmethoxy substituent enhances its lipophilicity and may influence its biological activity. This compound is typically used in medicinal chemistry and organic synthesis, where its unique structure can facilitate the development of pharmaceuticals or agrochemicals. Additionally, the presence of the boronic acid group allows for further functionalization and modification, making it a versatile building block in synthetic chemistry. Its solubility and stability in various solvents can vary, and it may exhibit specific reactivity patterns due to the electron-withdrawing nature of the boron atom. Overall, 6-(cyclopropylmethoxy)pyridine-3-boronic acid is a valuable compound in the field of organic synthesis and drug development.
Formula:C9H12BNO3
Synonyms:
  • Boronic acid, B-[6-(cyclopropylmethoxy)-3-pyridinyl]-
  • 6-(Cyclopropylmethoxy)pyridin-3-ylboronic acid
  • 2-(Cyclopropylmethoxy)pyridin-5-ylboronic acid
  • 6-(cyclopropylmethoxy)pyridine-3-boronic acid
  • 2-(Cyclopropylmethoxy)pyridine-5-boronic acid
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