The chemical substance with the name "Phenol, 3-[[[2-[4-hydroxy-5-methyl-2-(1-methylethyl)phenoxy]ethyl]methylamino]methyl]-4-methoxy-2,5,6-trimethyl-" and CAS number 171277-06-8 is a complex organic compound characterized by its phenolic structure, which includes multiple functional groups such as hydroxyl, methoxy, and amine. This compound is likely to exhibit properties typical of phenolic compounds, including potential antioxidant activity and the ability to participate in hydrogen bonding due to the presence of hydroxyl groups. Its structure suggests it may have applications in pharmaceuticals or as a biochemical probe, given the presence of various substituents that can influence its reactivity and solubility. The presence of multiple methyl groups may enhance lipophilicity, affecting its bioavailability and interaction with biological systems. Additionally, the compound's intricate structure may lead to unique physical and chemical properties, such as specific melting and boiling points, solubility in organic solvents, and potential reactivity with other chemical species.

Phenol, 3-[[[2-[4-hydroxy-5-methyl-2-(1-methylethyl)phenoxy]ethyl]methylamino]methyl]-4-methoxy-2,5,6-trimethyl-

171277-06-8: The chemical substance with the name "Phenol, 3-[[[2-[4-hydroxy-5-methyl-2-(1-methylethyl)phenoxy]ethyl]methylamino]methyl]-4-methoxy-2,5,6-trimethyl-" and CAS number 171277-06-8 is a complex organic compound characterized by its phenolic structure, which includes multiple functional groups such as hydroxyl, methoxy, and amine. This compound is likely to exhibit properties typical of phenolic compounds, including potential antioxidant activity and the ability to participate in hydrogen bonding due to the presence of hydroxyl groups. Its structure suggests it may have applications in pharmaceuticals or as a biochemical probe, given the presence of various substituents that can influence its reactivity and solubility. The presence of multiple methyl groups may enhance lipophilicity, affecting its bioavailability and interaction with biological systems. Additionally, the compound's intricate structure may lead to unique physical and chemical properties, such as specific melting and boiling points, solubility in organic solvents, and potential reactivity with other chemical species.

<p>JTH-601 free base is an antagonist of alpha 1 adrenergic receptor.</p>

CAS 171277-06-8

Phenol, 3-[[[2-[4-hydroxy-5-methyl-2-(1-methylethyl)phenoxy]ethyl]methylamino]methyl]-4-methoxy-2,5,6-trimethyl-

JTH-601 free base

Ref: TM-T24220