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CAS 119771-23-2

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N-(tert-Butoxycarbonyl)-4-(dihydroxyboryl)-L-phenylalanine

Description:
N-(tert-Butoxycarbonyl)-4-(dihydroxyboryl)-L-phenylalanine, commonly referred to as Boc-L-Phe(B(OH)2), is an amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group and a dihydroxyboron functional group attached to the phenylalanine backbone. This compound is typically used in organic synthesis and peptide chemistry, particularly for the introduction of boron-containing moieties into peptides, which can facilitate various chemical transformations or serve as a tool for bioconjugation. The Boc group provides stability and protects the amino group during synthesis, while the dihydroxyboron moiety can participate in reactions such as Suzuki coupling or serve as a reactive site for further modifications. The compound is generally soluble in organic solvents and may exhibit specific reactivity patterns due to the presence of both the boron and amino acid functionalities. Its applications extend to medicinal chemistry and materials science, where boron-containing compounds are of interest for their unique properties.
Formula:C14H20BNO6
Synonyms:
  • Boc-4-Borono-L-Phenylalanine
  • N-Boc-4-borono-L-phenylalanine
  • N-(tert-Butoxycarbonyl)-4-(dihydroxyboryl)-L-phenylalanine
  • (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-[4-(dihydroxyboranyl)phenyl]propanoic acid
  • EOS-61314
  • (S)-3-(4-boronophenyl)-2-((tert-butoxycarbonyl)amino)propanoicacid
  • Exit [Product Synonyms] (S)-3-(4-boronophenyl)-2-((tert-butoxycarbonyl)amino)propanoicacid
  • L-Phenylalanine, 4-borono-N-[(1,1-dimethylethoxy)carbonyl]-
  • (S)-3-(4-BORONOPHENYL)-2-(TERT-BUTOXYCARBONYL)PROPANOIC ACID
  • N-(tert-butoxycarbonyl)-4-(dihydroxyboryl)-1-phenylalanine
  • 4-Borono-N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine
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