This compound is a protected aspartic acid derivative used in peptide synthesis. It features a tert-butyl ester protecting group on the side chain and a benzyloxycarbonyl (Cbz) protecting group on the amino function, making it suitable for stepwise construction of peptides in research and manufacturing settings.
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.
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Boc-L-aspartic acid 4-benzyl ester
pharmaceutical intermediate
Boc-D-aspartic acid 4-benzyl ester
pharmaceutical intermediate
N'-Fmoc-N-Cbz-L-Lysine
pharmaceutical intermediate
O-(1,1-Dimethylethyl)-N-[(phenylmethoxy)carbonyl]-L-tyrosine
pharmaceutical intermediate
2-(4-Chlorophenyl)-3-oxopentanenitrile
pharmaceutical intermediate
(4-Chlorophenyl)(2-ethyl-1,3-dioxolan-2-yl)acetonitrile
pharmaceutical intermediate
4-chloro-7-methoxy-6-nitroquinazoline
pharmaceutical intermediate
The international HS code for 4-tert-Butyl hydrogen N-((phenylmethoxy)carbonyl)-L-aspartate (CAS 5545-52-8) 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)-4-[(2-methylpropan-2-yl)oxy]-4-oxo-2-(phenylmethoxycarbonylamino)butanoic acid
HLSLRFBLVZUVIE-LBPRGKRZSA-N
CC(C)(C)OC(=O)C[C@@H](C(=O)O)NC(=O)OCC1=CC=CC=C1
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