The chemical substance known as [(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4R)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic Acid 1,1-tert-Butyl Ester, with CAS number 900811-52-1, is a complex organic compound characterized by its multi-functional structure. It features a carbamic acid derivative, which is typically associated with biological activity, particularly in medicinal chemistry. The presence of methoxy and propoxy groups suggests potential for solubility in organic solvents and possible interactions with biological targets. The stereochemistry indicated by the (1S,3S) and (2S,4R) designations implies that the compound has specific three-dimensional orientations that can influence its reactivity and biological interactions. Additionally, the tert-butyl ester moiety enhances stability and may improve pharmacokinetic properties. Overall, this compound's intricate structure suggests potential applications in pharmaceuticals, particularly in the development of therapeutic agents. However, detailed studies would be necessary to fully elucidate its properties and biological effects.

[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4R)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic Acid 1,1-tert-Butyl Ester

900811-52-1: The chemical substance known as [(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4R)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic Acid 1,1-tert-Butyl Ester, with CAS number 900811-52-1, is a complex organic compound characterized by its multi-functional structure. It features a carbamic acid derivative, which is typically associated with biological activity, particularly in medicinal chemistry. The presence of methoxy and propoxy groups suggests potential for solubility in organic solvents and possible interactions with biological targets. The stereochemistry indicated by the (1S,3S) and (2S,4R) designations implies that the compound has specific three-dimensional orientations that can influence its reactivity and biological interactions. Additionally, the tert-butyl ester moiety enhances stability and may improve pharmacokinetic properties. Overall, this compound's intricate structure suggests potential applications in pharmaceuticals, particularly in the development of therapeutic agents. However, detailed studies would be necessary to fully elucidate its properties and biological effects.

CAS 900811-52-1

[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4R)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic Acid 1,1-tert-Butyl Ester