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CAS 261380-31-8

:

N-(tert-butoxycarbonyl)-2,5-difluoro-D-phenylalanine

Description:
N-(tert-butoxycarbonyl)-2,5-difluoro-D-phenylalanine, with the CAS number 261380-31-8, is an amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group on the amino group of the phenylalanine structure. This compound features two fluorine atoms substituted at the 2 and 5 positions of the aromatic ring, which can influence its electronic properties and reactivity. The Boc group is commonly used in peptide synthesis to protect the amino group during chemical reactions, allowing for selective modifications of other functional groups. The presence of fluorine atoms can enhance the lipophilicity and metabolic stability of the compound, making it of interest in medicinal chemistry and drug design. Additionally, the D-configuration of the amino acid indicates that it is a non-natural isomer, which may exhibit different biological activities compared to its L-counterpart. Overall, this compound's unique structural features make it a valuable building block in the synthesis of peptides and other bioactive molecules.
Formula:C14H17F2NO4
InChI:InChI=1/C14H17F2NO4/c1-14(2,3)21-13(20)17-11(12(18)19)7-8-6-9(15)4-5-10(8)16/h4-6,11H,7H2,1-3H3,(H,17,20)(H,18,19)/t11-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](Cc1cc(ccc1F)F)C(=O)O)O
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