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CAS 198545-59-4

:

FMOC-D-3,4-Difluorophe

Description:
FMOC-D-3,4-Difluorophenylalanine, identified by its CAS number 198545-59-4, is a derivative of the amino acid phenylalanine, modified with a 9-fluorenylmethoxycarbonyl (FMOC) protecting group and two fluorine atoms at the 3 and 4 positions of the phenyl ring. This compound is typically utilized in peptide synthesis and research due to its ability to enhance the stability and solubility of peptides during synthesis. The presence of fluorine atoms can also influence the electronic properties and reactivity of the molecule, making it valuable in medicinal chemistry and drug design. FMOC-D-3,4-Difluorophenylalanine is generally characterized by its solid state at room temperature, and it is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dichloromethane. Its unique structural features allow for specific interactions in biological systems, making it a useful tool in the study of protein structure and function. Safety data sheets should be consulted for handling and storage guidelines, as with all chemical substances.
Formula:C24H19F2NO4
InChI:InChI=1/C24H19F2NO4/c25-20-10-9-14(11-21(20)26)12-22(23(28)29)27-24(30)31-13-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-11,19,22H,12-13H2,(H,27,30)(H,28,29)/t22-/m1/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@H](Cc1ccc(c(c1)F)F)C(=O)O)O
Synonyms:
  • 3,4-Difluoro-D-Phenylalanine, Fmoc Protected
  • Fmoc-3,4-Difluoro-D-Phenylalanine
  • Fmoc-3,4-Difluoro-D-Phe-Oh
  • Fluorenylmethoxycarbonyl-D-3,4-difluorophenylalanine
  • Fmoc-D-3,4-Difluorophenylalanine
  • Fmoc-D-Phe(M,P-F2)-Oh
  • Fmoc-D-Phe(3,4-DiF)-OH
  • N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3,4-difluoro-D-phenylalanine
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