N-(4-Carboxybutanoyl)glycyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-L-argininamide hydrochloride (1:1)(CAS: 103213-40-7)

N-(4-Carboxybutanoyl)glycyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-L-argininamide hydrochloride is a crystalline compound. Its molecular weight is approximately 793.7 g/mol. It has a high solubility in water and low solubility in organic solvents. It is relatively stable under normal conditions but can react with bases to form the corresponding amide. It exhibits weak basicity due to the presence of the hydrochloride ion.

N-(4-Carboxybutanoyl)glycyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-L-argininamide hydrochloride can be synthesized via the amidation of N-(4-carboxybutanoyl)glycyl-L-arginine with 7-methoxy-2-oxo-2H-chromene, followed by the addition of hydrochloric acid to form the hydrochloride salt. The reaction is catalyzed by a mild coupling reagent, and the yield is typically around 75-85%. The reaction is carried out under mild conditions to maintain the stability of the chromenone ring.

N-(4-Carboxybutanoyl)glycyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-L-argininamide hydrochloride finds applications in pharmaceuticals, where it is used as a potential drug candidate for targeting specific biological pathways. It is also utilized in the preparation of advanced materials and sensors, due to its chromenone structure, which can be used in photochemical applications and sensing technologies.

When handling N-(4-Carboxybutanoyl)glycyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-L-argininamide hydrochloride, it is crucial to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. The compound should be stored in a fume hood to minimize exposure to air and moisture. In case of a spill, it should be handled with care and cleaned up using appropriate methods, as detailed in the safety data sheet (SDS). Always follow laboratory safety guidelines and handle with caution to avoid potential health hazards.