2-(2,4-Dichloro-phenyl)-6-fluoro-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid is a chemical compound characterized by its complex structure, which includes a tetrahydroisoquinoline core substituted with a dichlorophenyl group and a fluorine atom. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential biological activity. The presence of the carboxylic acid functional group suggests it may engage in hydrogen bonding and participate in acid-base reactions. The dichloro and fluoro substituents can influence the compound's lipophilicity, reactivity, and overall pharmacological profile. Such compounds are often studied for their potential therapeutic applications, particularly in medicinal chemistry, where modifications to the isoquinoline structure can lead to varied biological effects. Additionally, the specific arrangement of substituents can affect the compound's interaction with biological targets, making it a subject of interest in drug discovery and development. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental conditions and the presence of other chemical species.

2-(2,4-DICHLORO-PHENYL)-6-FLUORO-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-1-CARBOXYLIC ACID

1260637-71-5: 2-(2,4-Dichloro-phenyl)-6-fluoro-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid is a chemical compound characterized by its complex structure, which includes a tetrahydroisoquinoline core substituted with a dichlorophenyl group and a fluorine atom. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential biological activity. The presence of the carboxylic acid functional group suggests it may engage in hydrogen bonding and participate in acid-base reactions. The dichloro and fluoro substituents can influence the compound's lipophilicity, reactivity, and overall pharmacological profile. Such compounds are often studied for their potential therapeutic applications, particularly in medicinal chemistry, where modifications to the isoquinoline structure can lead to varied biological effects. Additionally, the specific arrangement of substituents can affect the compound's interaction with biological targets, making it a subject of interest in drug discovery and development. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental conditions and the presence of other chemical species.

<p>2-(2,4-Dichlorophenyl)-6-fluoro-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid</p>

CAS 1260637-71-5

2-(2,4-DICHLORO-PHENYL)-6-FLUORO-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-1-CARBOXYLIC ACID

2-(2,4-Dichlorophenyl)-6-fluoro-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid

Ref: 54-PC106713