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CAS 273221-71-9

:

4-Borono-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine

Description:
4-Borono-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine, with the CAS number 273221-71-9, is a synthetic amino acid derivative that incorporates a boronic acid functional group. This compound is characterized by its unique structure, which includes a phenylalanine backbone modified with a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis. The presence of the boronic acid moiety allows for potential applications in bioconjugation and drug delivery, as boron-containing compounds can interact with diols and other biomolecules. The Fmoc group provides stability during synthesis and can be removed under basic conditions to expose the amino group for further reactions. This compound is typically utilized in research settings, particularly in the fields of medicinal chemistry and peptide synthesis, due to its ability to facilitate the formation of complex molecular structures. Its solubility and reactivity are influenced by the functional groups present, making it a versatile building block in organic synthesis and pharmaceutical development.
Formula:C24H22BNO6
InChI:InChI=1S/C24H22BNO6/c27-23(28)22(13-15-9-11-16(12-10-15)25(30)31)26-24(29)32-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22,30-31H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1
InChI key:InChIKey=KQZPZGIZOXMZJP-QFIPXVFZSA-N
SMILES:C(OC(N[C@@H](CC1=CC=C(B(O)O)C=C1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • Fmoc-4-borono-L-phenylalanine
  • 4-Borono-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
  • L-Phenylalanine, 4-borono-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
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