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CAS 1421846-79-8

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3-Methylisoxazole-4-boronic Acid Pinacol Ester

Description:
3-Methylisoxazole-4-boronic Acid Pinacol Ester is a chemical compound characterized by its unique structure, which includes a boronic acid moiety and an isoxazole ring. The compound features a methyl group at the 3-position of the isoxazole, contributing to its reactivity and potential applications in organic synthesis. Boronic acids are known for their ability to form reversible covalent bonds with diols, making this ester particularly useful in cross-coupling reactions and as a building block in the synthesis of various organic compounds. The pinacol ester form enhances its stability and solubility, facilitating its use in various chemical reactions. This compound is often utilized in medicinal chemistry and materials science due to its functional properties. Additionally, it may exhibit specific reactivity patterns typical of boron-containing compounds, such as participation in Suzuki-Miyaura coupling reactions. Overall, 3-Methylisoxazole-4-boronic Acid Pinacol Ester is a versatile intermediate in synthetic organic chemistry, with potential applications in drug development and the creation of complex molecular architectures.
Formula:C10H16BNO3
Synonyms:
  • Isoxazole, 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-oxazole
  • 3-Methylisoxazole-4-boronic Acid Pinacol Ester
  • 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoxazole
  • 3-Methylisoxazole-4-boronic Acid Pinacol Este
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90
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