CAS 223581-83-7
:FMOC-L-PRO(4-OXO)
Description:
FMOC-L-PRO(4-OXO), also known as 4-oxo-2-(9-fluorenylmethoxycarbonyl)-L-proline, is a chemical compound commonly used in peptide synthesis and research. It features a fluorenylmethoxycarbonyl (FMOC) protecting group, which is widely utilized to protect amino groups during the synthesis of peptides. The presence of the 4-oxo group indicates that it has a ketone functional group, contributing to its reactivity and stability in various chemical environments. This compound is typically characterized by its solid state at room temperature and is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dichloromethane. Its molecular structure allows for specific interactions in biochemical applications, making it valuable in the development of peptide-based drugs and materials. Additionally, FMOC-L-PRO(4-OXO) is often used in solid-phase peptide synthesis, where the FMOC group can be easily removed under basic conditions, facilitating the sequential addition of amino acids. Overall, its unique structural features and functional groups make it an important tool in organic and medicinal chemistry.
Formula:C20H17NO5
Synonyms:- FMOC-S-PRO(4-OXO)-OH
- Fmoc-Pro(4-keto)
- 1-Fmoc-4-oxo-L-proline
- (S)-FMOC-4-OXO-PROLINE
- Fmoc-Pro(4-keto)-OH≥ 99% (HPLC)
- (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-oxopyrrolidine-2-carboxylic acid
- (S)-N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-4-OXO-PROLINE
- Fmoc-L-Pro(4-keto)-OH
- FMOC-L-PRO(4-OXO)
- (2S)-1-{[(9H-fluoren-9-yl)methoxy]carbonyl}-4-oxopyrrolidine-2-carboxylic acid
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