N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-(2-quinolinyl)-D-alanine(CAS: 214852-58-1)

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-(2-quinolinyl)-D-alanine (CAS: 214852-58-1) is a crystalline solid with a molecular weight of approximately 461.4 g/mol. It is slightly water-soluble and stable under normal conditions. The compound reacts readily with nucleophiles due to its ester and amide functionalities. It has a high boiling point and is resistant to thermal and oxidative degradation.

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-(2-quinolinyl)-D-alanine is typically synthesized through multistep organic reactions, including protected amino acid synthesis and amidation. The key steps involve the formation of a fluorenylmethoxycarbonyl (Fmoc) protected derivative and subsequent coupling with 2-quinolinyl-D-alanine. The reaction is often catalyzed by a suitable coupling reagent such as HATU and performed under anhydrous conditions to ensure high yield and selectivity.

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-(2-quinolinyl)-D-alanine (CAS: 214852-58-1) is primarily used in the pharmaceutical industry for the development of new drugs. It is also utilized in the preparation of organic semiconductors and photovoltaic materials. Additionally, it can be employed in the synthesis of complex molecules for research purposes and in the development of advanced sensor technologies.

When handling N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-(2-quinolinyl)-D-alanine (CAS: 214852-58-1), it is important to use appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats. Work should be conducted in a well-ventilated area or fume hood. Spills should be handled with care using appropriate absorbent materials and should be cleaned up promptly. Always refer to the Safety Data Sheet (SDS) for detailed information on safe handling and storage.