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CAS 167993-07-9

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N-[(1,1-Dimethylethoxy)carbonyl]-2,6-difluoro-L-phenylalanine

Description:
N-[(1,1-Dimethylethoxy)carbonyl]-2,6-difluoro-L-phenylalanine, with CAS number 167993-07-9, is a synthetic amino acid derivative characterized by the presence of a difluorophenyl group and a tert-butoxycarbonyl (Boc) protecting group. This compound features a chiral center, making it optically active, and is typically utilized in peptide synthesis and medicinal chemistry due to its potential biological activity. The difluoro substitution on the phenyl ring can enhance the compound's lipophilicity and influence its interaction with biological targets. The Boc group serves as a protective moiety that can be removed under specific conditions, allowing for further functionalization or incorporation into larger peptide structures. The compound's stability, solubility, and reactivity are influenced by its functional groups, making it a valuable intermediate in the development of pharmaceuticals and research applications. Overall, its unique structural features contribute to its utility in various chemical and biological contexts.
Formula:C14H17F2NO4
InChI:InChI=1S/C14H17F2NO4/c1-14(2,3)21-13(20)17-11(12(18)19)7-8-9(15)5-4-6-10(8)16/h4-6,11H,7H2,1-3H3,(H,17,20)(H,18,19)/t11-/m0/s1
InChI key:InChIKey=JQRFXXIFWMNGAG-NSHDSACASA-N
SMILES:C([C@H](NC(OC(C)(C)C)=O)C(O)=O)C1=C(F)C=CC=C1F
Synonyms:
  • N-[(1,1-Dimethylethoxy)carbonyl]-2,6-difluoro-L-phenylalanine
  • N-BOC-L-2,6-difluorophenylalanine
  • L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2,6-difluoro-
  • (2s)-3-(2,6-Difluorophenyl)-2-[(tert-butoxy)carbonylamino]propanoic acid
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