This compound is an Fmoc-protected derivative of glutamine featuring a trityl (Trt) protecting group on the side-chain amide. It is primarily used in solid-phase peptide synthesis as a building block for incorporating glutamine residues.
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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Fmoc-N-trityl-L-asparagine
pharmaceutical intermediate
N-(9-Fluorenylmethyloxycarbonyl)-N'-trityl-D-asparagine
pharmaceutical intermediate
Fmoc-L-glutamic acid 1-allyl ester
research compound
N²-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-L-α-glutamine
research compound
(R)-Nomega-(t-Butoxycarbonyl)-Nalpha-(9-fluorenylmethoxycarbonyl)-alpha-methylornithin
research compound
(alphaS)-alpha-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1H-Pyrrolo[2,3-b]pyridine-3-propanoic acid
research compound
Neohesperidin
research compound
3'-o-amino-2'-deoxyadenosine
research compound
The international HS code for (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-[(triphenylmethyl)carbamoyl]butanoic acid (CAS 132327-80-1) 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-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-(tritylamino)pentanoic acid
WDGICUODAOGOMO-DHUJRADRSA-N
C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)NC(=O)CC[C@@H](C(=O)O)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46
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