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CAS 1449135-41-4

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5-(N-BOC-Amino)-2-fluorophenylboronic acid, pinacol ester

Description:
5-(N-BOC-Amino)-2-fluorophenylboronic acid, pinacol ester, is a chemical compound characterized by its boronic acid functionality, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis and medicinal chemistry. The presence of the N-Boc (tert-butoxycarbonyl) protecting group on the amino group enhances the compound's stability and solubility, making it suitable for various reactions, including Suzuki coupling. The fluorine atom in the 2-position of the phenyl ring can influence the electronic properties and reactivity of the compound, potentially enhancing its biological activity. The pinacol ester moiety contributes to the compound's stability and can facilitate its use in further synthetic transformations. Overall, this compound is valuable in the development of pharmaceuticals and agrochemicals, particularly in the synthesis of complex organic molecules. Its unique structural features make it a versatile intermediate in chemical research and development.
Formula:C17H25BFNO4
Synonyms:
  • 5-(N-BOC-Amino)-2-fluorophenylboronic acid, pinacol ester
  • Carbamic acid, N-[4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, 1,1-dimethylethyl ester
  • tert-butyl N-(4-fluoro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
  • tert-Butyl (4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
  • tert-butyl N-[4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
  • (5-((TERT-BUTOXYCARBONYL)AMINO)-2-FLUOROPHENYL)BORONIC ACID PINACOL ESTER
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