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CAS 1158984-94-1

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N-Boc-pyrrole-2-boronic acid MIDA ester

Description:
N-Boc-pyrrole-2-boronic acid MIDA ester is a specialized chemical compound used primarily in organic synthesis and medicinal chemistry. It features a pyrrole ring, which is a five-membered aromatic heterocycle containing nitrogen, and is protected by a tert-butyloxycarbonyl (Boc) group, enhancing its stability and solubility. The presence of a boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable for constructing complex organic molecules. The MIDA (MIDA = boronic acid) ester functionality provides a unique advantage, as it can be easily converted to the corresponding boronic acid under mild conditions, facilitating further reactions. This compound is typically characterized by its solid-state properties, including melting point and solubility in organic solvents. Its reactivity profile is influenced by the electron-rich nature of the pyrrole ring and the boron center, making it a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data should be consulted for handling, as with all boron-containing compounds, due to potential toxicity and environmental considerations.
Formula:C14H19BN2O6
Synonyms:
  • 1-(tert-Butoxycarbonyl)pyrrole-2-boronic acid MIDA ester
  • Tert-Butyl 2-(6-Methyl-4,8-Dioxo-1,3,6,2-Dioxazaborocan-2-Yl)Pyrrole-1-Carboxylate
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