This compound is a protected adamantyl amino acid derivative used as a building block in peptide synthesis. Its structure incorporates a tert-butoxycarbonyl (Boc) protecting group and an adamantane cage, making it valuable for introducing sterically hindered amino acid residues into peptides.
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-3-Hydroxy-1-adamantyl-D-glycine
pharmaceutical intermediate
N-Boc-O-Benzyl-D-serine
research compound
N-BOC-L-Prolinal
research compound
Fmoc-Tyr(tBu)-Ser(Psi(Me,Me)pro)-OH
research compound
N-Cbz-D-Alanine
research compound
N-acetylmannosamine
research compound
2,6-Dimethyl-4-methoxyphenylboronic acid
research compound
3-Bromo-2-fluoropyridine
research compound
(2S)-2-(1-adamantyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
LJUATQZYDYSZPV-CQCMJFKXSA-N
CC(C)(C)OC(=O)N[C@H](C(=O)O)C12CC3CC(C1)CC(C3)C2
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