Ethyl 2-(4-fluoro-phenyl)-6-methoxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylate is a chemical compound characterized by its complex structure, which includes an isoquinoline core, a methoxy group, and a fluorophenyl substituent. This compound typically exhibits properties associated with isoquinoline derivatives, such as potential biological activity, including analgesic or anti-inflammatory effects. The presence of the ethyl ester functional group suggests it may have moderate solubility in organic solvents and could participate in various chemical reactions, including hydrolysis. The fluorine atom in the para position of the phenyl ring may enhance lipophilicity and influence the compound's pharmacokinetic properties. Additionally, the methoxy group can affect the electronic distribution within the molecule, potentially impacting its reactivity and interaction with biological targets. Overall, this compound's unique structural features may contribute to its potential applications in medicinal chemistry and drug development, although specific biological activities would require further investigation.

ETHYL 2-(4-FLUORO-PHENYL)-6-METHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-1-CARBOXYLATE

1260642-17-8: Ethyl 2-(4-fluoro-phenyl)-6-methoxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylate is a chemical compound characterized by its complex structure, which includes an isoquinoline core, a methoxy group, and a fluorophenyl substituent. This compound typically exhibits properties associated with isoquinoline derivatives, such as potential biological activity, including analgesic or anti-inflammatory effects. The presence of the ethyl ester functional group suggests it may have moderate solubility in organic solvents and could participate in various chemical reactions, including hydrolysis. The fluorine atom in the para position of the phenyl ring may enhance lipophilicity and influence the compound's pharmacokinetic properties. Additionally, the methoxy group can affect the electronic distribution within the molecule, potentially impacting its reactivity and interaction with biological targets. Overall, this compound's unique structural features may contribute to its potential applications in medicinal chemistry and drug development, although specific biological activities would require further investigation.

<p>Ethyl 2-(4-fluorophenyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylate</p>

CAS 1260642-17-8

ETHYL 2-(4-FLUORO-PHENYL)-6-METHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-1-CARBOXYLATE

Ethyl 2-(4-fluorophenyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline-1-carboxylate

Ref: 54-PC107999