For research use only. Not for therapeutic Use.
Cbz-Ala-Ala-Asn TFA(Cat No.:I041410)is a protected peptide derivative used in peptide synthesis and research. The “Cbz” (carbobenzoxy) group serves as a protective moiety for the amine group of alanine, preventing unwanted reactions during peptide assembly. This compound consists of two alanine residues and an asparagine residue, with TFA (trifluoroacetic acid) used for deprotection, aiding in the removal of the Cbz group. Cbz-Ala-Ala-Asn TFA is commonly used in the preparation of peptides for studying protein structure, interactions, and other biochemical applications, as well as in drug discovery research.
Synonyms | (2S)-4-amino-4-oxo-2-[[(2S)-2-[[(2S)-2-(phenylmethoxycarbonylamino)propanoyl]amino]propanoyl]amino]butanoic acid;2,2,2-trifluoroacetic acid |
Molecular Formula | C20H25F3N4O9 |
Purity | ≥95% |
IUPAC Name | (2S)-4-amino-4-oxo-2-[[(2S)-2-[[(2S)-2-(phenylmethoxycarbonylamino)propanoyl]amino]propanoyl]amino]butanoic acid;2,2,2-trifluoroacetic acid |
InChI | InChI=1S/C18H24N4O7.C2HF3O2/c1-10(16(25)22-13(17(26)27)8-14(19)23)20-15(24)11(2)21-18(28)29-9-12-6-4-3-5-7-12;3-2(4,5)1(6)7/h3-7,10-11,13H,8-9H2,1-2H3,(H2,19,23)(H,20,24)(H,21,28)(H,22,25)(H,26,27);(H,6,7)/t10-,11-,13-;/m0./s1 |
InChIKey | XHTNNYYTYDZFEL-SQRKDXEHSA-N |
SMILES | C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](C)NC(=O)OCC1=CC=CC=C1.C(=O)(C(F)(F)F)O |