The chemical substance known as (2R)-2-[(1R)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-phenylethanol, with the CAS number 548443-18-1, is a chiral compound characterized by its complex structure, which includes a tetrahydroisoquinoline moiety and a phenylethanol group. This compound exhibits stereochemistry, with specific configurations at its chiral centers, influencing its biological activity and interactions. It is typically soluble in organic solvents and may exhibit moderate solubility in water, depending on the pH and other conditions. The presence of methoxy groups contributes to its potential for hydrogen bonding and affects its electronic properties. This compound may be of interest in medicinal chemistry due to its structural features, which could relate to various pharmacological activities. Its synthesis and characterization would involve standard organic chemistry techniques, including chiral resolution methods if necessary. Overall, the compound's unique structural attributes suggest potential applications in drug development and research in the field of organic and medicinal chemistry.

(2R)-2-[(1R)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-phenylethanol

548443-18-1: The chemical substance known as (2R)-2-[(1R)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-phenylethanol, with the CAS number 548443-18-1, is a chiral compound characterized by its complex structure, which includes a tetrahydroisoquinoline moiety and a phenylethanol group. This compound exhibits stereochemistry, with specific configurations at its chiral centers, influencing its biological activity and interactions. It is typically soluble in organic solvents and may exhibit moderate solubility in water, depending on the pH and other conditions. The presence of methoxy groups contributes to its potential for hydrogen bonding and affects its electronic properties. This compound may be of interest in medicinal chemistry due to its structural features, which could relate to various pharmacological activities. Its synthesis and characterization would involve standard organic chemistry techniques, including chiral resolution methods if necessary. Overall, the compound's unique structural attributes suggest potential applications in drug development and research in the field of organic and medicinal chemistry.

<p>(R*)-2-((R*)-6,7-Dimethoxy-1,2,3,4-tetrahydro-isoquinolin-1-yl)-2-phenyl-ethanol</p>

CAS 548443-18-1

(2R)-2-[(1R)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-phenylethanol

(R)-2-((R)-6,7-Dimethoxy-1,2,3,4-tetrahydro-isoquinolin-1-yl)-2-phenyl-ethanol

Ref: 54-OR307634