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CAS 1072944-98-9

:

1-BOC-Pyrrole-2-boronic acid, pinacol ester

Description:
1-BOC-Pyrrole-2-boronic acid, pinacol ester, identified by CAS number 1072944-98-9, is a chemical compound that features a pyrrole ring substituted with a boronic acid moiety and a tert-butyloxycarbonyl (BOC) protecting group. This compound is characterized by its boron-containing functional group, which is known for its utility in cross-coupling reactions, particularly in the synthesis of complex organic molecules. The BOC group serves as a protective group for amines, allowing for selective reactions without interference from the amine functionality. The pinacol ester formation enhances the stability and solubility of the boronic acid, making it more amenable for various synthetic applications. Typically, this compound is used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in Suzuki-Miyaura coupling reactions. Its properties, such as solubility and reactivity, can be influenced by the presence of the BOC and pinacol ester groups, making it a versatile intermediate in synthetic chemistry.
Formula:C15H24BNO4
Synonyms:
  • 1-(tert-Butoxycarbonyl)-1H-pyrrole-2-boronic acid pinacol ester
  • tert-butyl 2-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate
  • 1-N-BOC-pyrrole-2-boronic acid, pinacol ester
  • tert-butyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrole-1-carboxylate
  • 1-BOC-PYRROLE-2-BORONIC ACID, PINACOL ESTER
  • 1-Boc-Pyrrole-2-Boronic Acid, Pinacol Ester
  • N-Boc-pyrrole-2-boronic Acid Pinacol Ester
  • -1H-pyrrole-1-carboxylate
  • T-BUTYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-PYRROLE-1-CARBOXYLATE
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