(4S)-4-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-[(2-methyl-2-propanyl)oxy]-5-oxopentanoic acid(CAS: 84793-07-7)

This compound is a complex organic molecule with the CAS number 84793-07-7. It features a pentanoic acid backbone with a 5-oxo group, an amino group protected by a fluoren-9-ylmethoxy carbonyl (Fmoc) moiety, and a tert-butyl ether substituent. Its stereochemistry is defined by the (4S) configuration, making it a key intermediate in pharmaceutical synthesis and molecular research. The structure combines aromatic, aliphatic, and functional groups, contributing to its reactivity and utility in chemical processes.

This compound is primarily used in pharmaceutical research as a protected amino acid derivative, enabling controlled functionalization in drug molecule synthesis. It serves as an intermediate in the development of bioactive compounds and is also employed in organic chemistry for structural studies. Its unique Fmoc group and tert-butyl protection make it valuable in peptide chemistry and advanced chemical applications.

Safety data for this compound is limited, but as a chemical reagent, it requires standard laboratory precautions. It may pose mild irritation risks upon contact with skin or eyes, and inhalation should be avoided. Always handle it with gloves, safety goggles, and in a well-ventilated area. Adherence to OSHA and EPA guidelines is recommended for safe use and disposal.

Store this compound in a cool, dry place (ideally below 25°C), away from light, and in airtight containers to prevent moisture absorption. Ensure it is kept in a chemically inert environment to maintain stability. Avoid exposure to strong oxidizers or incompatible substances. Regularly check storage conditions to preserve its integrity and prolong shelf life.