Bis-(3-butyryl-2,6-dihydroxy-4-methoxy-5-methyl-phenyl)-methane, with the CAS number 478-28-4, is an organic compound characterized by its complex molecular structure, which includes multiple functional groups. This substance features two butyryl groups attached to a central methane bridge, along with dihydroxy and methoxy substituents on the aromatic rings. The presence of hydroxyl groups contributes to its potential solubility in polar solvents and may influence its reactivity, particularly in hydrogen bonding and redox reactions. The methoxy group can enhance the compound's lipophilicity, affecting its biological activity and interaction with other molecules. This compound may exhibit antioxidant properties due to the presence of hydroxyl groups, making it of interest in various fields, including pharmaceuticals and materials science. Its specific applications and behavior in chemical reactions would depend on the context of use, including concentration, solvent, and environmental conditions. Overall, the unique combination of functional groups in this compound suggests a diverse range of potential applications and biological activities.

bis-(3-butyryl-2,6-dihydroxy-4-methoxy-5-methyl-phenyl)-methane

478-28-4: Bis-(3-butyryl-2,6-dihydroxy-4-methoxy-5-methyl-phenyl)-methane, with the CAS number 478-28-4, is an organic compound characterized by its complex molecular structure, which includes multiple functional groups. This substance features two butyryl groups attached to a central methane bridge, along with dihydroxy and methoxy substituents on the aromatic rings. The presence of hydroxyl groups contributes to its potential solubility in polar solvents and may influence its reactivity, particularly in hydrogen bonding and redox reactions. The methoxy group can enhance the compound's lipophilicity, affecting its biological activity and interaction with other molecules. This compound may exhibit antioxidant properties due to the presence of hydroxyl groups, making it of interest in various fields, including pharmaceuticals and materials science. Its specific applications and behavior in chemical reactions would depend on the context of use, including concentration, solvent, and environmental conditions. Overall, the unique combination of functional groups in this compound suggests a diverse range of potential applications and biological activities.

Pseudoaspidin

Pseudoaspidin is isolated from fern plants.

CAS 478-28-4

bis-(3-butyryl-2,6-dihydroxy-4-methoxy-5-methyl-phenyl)-methane

Pseudoaspidin

Ref: 7W-GY5937

Pseudoaspidin

Ref: TM-T3S1117

Pseudoaspidin

Ref: BP-BP3870