This compound is a protected derivative of the amino acid tyrosine, where the amino group is blocked by a tert-butoxycarbonyl (Boc) group and the phenolic hydroxyl is protected as a benzyl ether. It is used as a building block in solid-phase peptide synthesis, enabling the selective incorporation of tyrosine derivatives into peptide chains.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
Sourcing O-Benzyl-N-((tert-butoxy)carbonyl)-L-tyrosine?
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N-(tert-Butoxycarbonyl)-L-phenylalanine
pharmaceutical intermediate
Boc-D-Phenylalanine
research compound
Boc-O-ethyl-D-tyrosine
research compound
2-{2-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]acetamido}acetic acid
research compound
FMOC-PRO-THR(PSI(ME,ME)PRO)-OH
research compound
N-Cbz-N-methyl-L-leucine
research compound
N-Carbobenzyloxy-D-asparagine
research compound
5-Methyl-2-nitro-3-furancarboxaldehyde
research compound
The international HS code for O-Benzyl-N-((tert-butoxy)carbonyl)-L-tyrosine (CAS 2130-96-3) is 2924.29.
2924.29
2924 29 70
Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(4-phenylmethoxyphenyl)propanoic acid
ZAVSPTOJKOFMTA-SFHVURJKSA-N
CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)OCC2=CC=CC=C2)C(=O)O
Sourcing O-Benzyl-N-((tert-butoxy)carbonyl)-L-tyrosine?
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