Ethyl 2-(4-fluoro-phenyl)-6-hydroxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylate is a chemical compound characterized by its complex structure, which includes an isoquinoline core, a carboxylate ester functional group, and a fluorophenyl substituent. The presence of the hydroxy group contributes to its potential for hydrogen bonding, influencing its solubility and reactivity. The fluorine atom in the para position of the phenyl ring can enhance the compound's lipophilicity and may affect its biological activity by altering electronic properties. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas targeting neurological or psychiatric conditions, given the isoquinoline framework's historical association with various bioactive compounds. As with many organic compounds, its stability, reactivity, and interactions with biological systems would depend on environmental conditions such as pH, temperature, and the presence of other chemical species.

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

1260637-19-1: Ethyl 2-(4-fluoro-phenyl)-6-hydroxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylate is a chemical compound characterized by its complex structure, which includes an isoquinoline core, a carboxylate ester functional group, and a fluorophenyl substituent. The presence of the hydroxy group contributes to its potential for hydrogen bonding, influencing its solubility and reactivity. The fluorine atom in the para position of the phenyl ring can enhance the compound's lipophilicity and may affect its biological activity by altering electronic properties. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas targeting neurological or psychiatric conditions, given the isoquinoline framework's historical association with various bioactive compounds. As with many organic compounds, its stability, reactivity, and interactions with biological systems would depend on environmental conditions such as pH, temperature, and the presence of other chemical species.

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

CAS 1260637-19-1

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

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

Ref: 54-PC107998