Product Information
- (2R)-1-(9H-Fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid
- (2R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid
- (2R)-1-[[(9H-Fluoren-9-yl)methoxy]carbonyl]pyrrolidine-2-carboxylic acid
- (R)-1-[[(9H-Fluoren-9-yl)methoxy]carbonyl]pyrrolidine-2-carboxylic acid
- (R)-N-(9-Fluorenylmethoxycarbonyl)proline
- (R)-N-FMOC-proline
- 1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester, (2R)-
- 1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester, (R)-
- 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-proline
- 1-[[(9H-Fluoren-9-yl)methoxy]carbonyl]-<span class="text-smallcaps">D</span>-proline
- See more synonyms
- 300: PN: US20070042401 PAGE: 38 claimed protein
- 992: PN: WO2006135786 PAGE: 71 claimed protein
- N-(9-Fluorenylmethoxycarbonyl)-<span class="text-smallcaps">D</span>-proline
- N-alpha-(9-fluorenylmethyloxycarbonyl)-D-proline
Fmoc-D-Pro-OH is a building block for peptide synthesis. It is a protected form of proline with an amido group, which can be used to synthesize polypeptides. Fmoc-D-Pro-OH can be coupled with other amino acids using the aldol condensation or methodologies like the strategy of organocatalysts. This building block is also useful in the synthesis of macrocycles and cyclohexanones, which are aliphatic and cyclic compounds. The recoverable nature of Fmoc-D-Pro-OH allows it to be reused in multiple reactions, so it is an economical choice for Building Blocks.
Chemical properties
Technical inquiry about: 3D-FDP-1826-PI Fmoc-D-Pro-OH
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