顺式-Fmoc-Pro(4-N3)-OH;(2S,4S)-1-(((9H-芴-9-基)甲氧基)羰基)-4-叠氮吡咯烷-2-羧酸
cis-Fmoc-Pro(4-N3)-OH (Synonyms: Fmoc-(2S, 4S)-4-azidoproline; (2S,4S)-4-azido-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid; (2S,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-azidopyrrolidine-2-carboxylic acid)
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中文名称顺式-Fmoc-Pro(4-N3)-OH;(2S,4S)-1-(((9H-芴-9-基)甲氧基)羰基)-4-叠氮吡咯烷-2-羧酸
英文名称 cis-Fmoc-Pro(4-N3)-OH (Synonyms: Fmoc-(2S, 4S)-4-azidoproline; (2S,4S)-4-azido-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid; (2S,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-azidopyrrolidine-2-carboxylic acid)
CAS号263847-08-1
分子式C20H18N4O4
分子量378.38
MDLMFCD04115792
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A useful tool for the synthesis of branched, side-chain modified, cyclic peptides and peptide tools for click chemistry by Fmoc SPPS. The side-chain azido group is completely stable to piperidine and TFA, but can be readily converted to an amine on the solid phase or in solution by reduction with thiols or phosphines.

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