![Butanoic acid,2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-[[(2-propen-1-yloxy)carbonyl]amino]-,(…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F338703-butanoic-acid-2-9h-fluoren-9-ylmethoxy-carbonyl-amino-4-2-propen-1-yloxy-carbonyl-amino-2r.webp&w=3840&q=75)
CAS 387824-78-4
:Butanoic acid,2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-[[(2-propen-1-yloxy)carbonyl]amino]-,(2R)-
Description:
Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-[[(2-propen-1-yloxy)carbonyl]amino]-, (2R)-, is a complex organic compound characterized by its functional groups and structural features. It contains a butanoic acid moiety, which contributes to its acidic properties, and is further modified with two distinct amine functionalities. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates its use in peptide synthesis, as Fmoc is a common protecting group for amino acids. Additionally, the compound features a propenyloxycarbonyl group, which may impart unique reactivity or solubility characteristics. The (2R) designation suggests specific stereochemistry, indicating that the compound has a chiral center, which can influence its biological activity and interactions. Overall, this compound is likely to be of interest in medicinal chemistry and peptide synthesis due to its structural complexity and functional versatility. Its CAS number, 387824-78-4, allows for precise identification in chemical databases and literature.
Formula:C23H24N2O6
Synonyms:- Butanoicacid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-[[(2-propenyloxy)carbonyl]amino]-,(2R)-
- Fmoc-D-Dab(Aloc)-OH
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