The chemical substance known as (αS)-4-Hydroxy-3-methoxy-α-[(1R)-1-[2-methoxy-4-(1E)-1-propen-1-ylphenoxy]ethyl]benzenemethanol, with the CAS number 891182-94-8, is a complex organic compound characterized by its multi-functional structure. It features a phenolic hydroxyl group, a methoxy group, and an ethyl side chain that includes a propenyl group, contributing to its potential biological activity. The presence of stereocenters indicates that the compound can exist in different stereoisomeric forms, which may influence its pharmacological properties. This compound is likely to exhibit solubility in organic solvents due to its hydrophobic aromatic components, while the hydroxyl group may enhance its solubility in polar solvents. Its structural complexity suggests potential applications in medicinal chemistry, possibly as a lead compound for drug development. The specific interactions and reactivity of this substance would depend on its conformation and the functional groups present, making it a subject of interest for further research in fields such as pharmacology and organic synthesis.

(αS)-4-Hydroxy-3-methoxy-α-[(1R)-1-[2-methoxy-4-(1E)-1-propen-1-ylphenoxy]ethyl]benzenemethanol

891182-94-8: The chemical substance known as (αS)-4-Hydroxy-3-methoxy-α-[(1R)-1-[2-methoxy-4-(1E)-1-propen-1-ylphenoxy]ethyl]benzenemethanol, with the CAS number 891182-94-8, is a complex organic compound characterized by its multi-functional structure. It features a phenolic hydroxyl group, a methoxy group, and an ethyl side chain that includes a propenyl group, contributing to its potential biological activity. The presence of stereocenters indicates that the compound can exist in different stereoisomeric forms, which may influence its pharmacological properties. This compound is likely to exhibit solubility in organic solvents due to its hydrophobic aromatic components, while the hydroxyl group may enhance its solubility in polar solvents. Its structural complexity suggests potential applications in medicinal chemistry, possibly as a lead compound for drug development. The specific interactions and reactivity of this substance would depend on its conformation and the functional groups present, making it a subject of interest for further research in fields such as pharmacology and organic synthesis.

<p>Odoratisol B, a natural product, is isolated from Machilus odoratissima NEES [1].</p>

CAS 891182-94-8

(αS)-4-Hydroxy-3-methoxy-α-[(1R)-1-[2-methoxy-4-(1E)-1-propen-1-ylphenoxy]ethyl]benzenemethanol

Odoratisol B

Ref: TM-T81621