This compound is a research reagent used in peptide synthesis, specifically as a protected dipeptide building block. It consists of two proline residues with an Fmoc (fluorenylmethoxycarbonyl) protecting group and a free carboxylic acid, making it suitable for solid-phase peptide synthesis.
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 N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-prolinyl-L-proline?
Post a free purchase request — no account needed. It reaches suppliers of this product, and replies go straight to your inbox.
Fmoc-Pro-Pro-Pro-OH
research compound
(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid
pharmaceutical intermediate
Fmoc-D-proline
research compound
Fmoc-Ala-Pro-OH
research compound
N-[(tert-Butoxy)carbonyl]-L-tryptophan
research compound
Fmoc-L-glutamic acid 5-allyl ester
research compound
Fmoc-Gln(Trt)-Thr(Psi(Me,Me)pro)-OH
research compound
(R)-2-((R)-2-((R)-2-Acetamido-3-(naphthalen-2-yl)propanamido)-3-(4-chlorophenyl)propanamido)-3-(pyridin-3-yl)propanoic acid
research compound
(2S)-1-[(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid
VRAQFWSWKRNOGU-VXKWHMMOSA-N
C1C[C@H](N(C1)C(=O)[C@@H]2CCCN2C(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35)C(=O)O
Sourcing N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-prolinyl-L-proline?
Post a free purchase request — no account needed. It reaches suppliers of this product, and replies go straight to your inbox.