N-Boc-L-tyrosine

• CAT Number: R061328
• CAS Number: 3978-80-1
• Molecular Formula: C14H19NO5
• Molecular Weight: 281.31
• Purity: ≥95%
• Synonyms: N-[(1,1-Dimethylethoxy)carbonyl]-L-tyrosine; N-Carboxy-L-tyrosine N-tert-Butyl Ester; (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(4-hydroxyphenyl)propanoic Acid; (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(4-hydroxyphenyl)propanoic Acid; BOC-L-tyrosine; N-(ter
• Storage: -20°C
• IUPAC Name: (2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
• InChI: InChI=1S/C14H19NO5/c1-14(2,3)20-13(19)15-11(12(17)18)8-9-4-6-10(16)7-5-9/h4-7,11,16H,8H2,1-3H3,(H,15,19)(H,17,18)/t11-/m0/s1
• InChIKey: CNBUSIJNWNXLQQ-NSHDSACASA-N
• SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)O

N-Boc-L-tyrosine（Cat No.:R061328）is a protected form of the amino acid L-tyrosine, featuring a tert-butoxycarbonyl (Boc) group at the amino terminus. This protection prevents side reactions during peptide synthesis, making it ideal for solid-phase and solution-phase methods. The phenolic side chain remains available for selective modification, enabling incorporation into complex peptide structures and bioactive compounds. N-Boc-L-tyrosine plays a crucial role in pharmaceutical development, combinatorial chemistry, and protein engineering. Supplied at high purity, it is well-suited for research in medicinal chemistry, peptide synthesis, and biochemical pathway studies.