2-(2-chloroethyl)-3,4-dihydroisoquinoline
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- Molecular formula
- C11H12ClN
- CAS Number
- 65417-00-5
- IUPAC Name
- 2-(2-chloroethyl)-3,4-dihydro-1H-isoquinoline
- Molecular Weight
- 181.67g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1197g/cm3
- Synonyms
- 2-(2-chloroethyl)-3, 4-dihydro-1H-isoquinoline
Identification
Interesting facts
Interesting Facts about 2-(2-chloroethyl)-3,4-dihydro-1H-isoquinoline
2-(2-chloroethyl)-3,4-dihydro-1H-isoquinoline is a fascinating compound that showcases the intricacies of organic chemistry and medicinal applications. Here are some notable aspects:
- Structural Variety: This compound belongs to the class of isoquinolines, which are a significant structural motif in various natural products and pharmaceuticals.
- Biological Activity: Isoquinolines and their derivatives have been extensively studied for their biological activities, including roles as:
- Anticancer agents
- Antimicrobial compounds
- Antidepressants
- Chloroethyl Group: The presence of the chloroethyl group enhances the reactivity of the compound, making it a potential precursor for various synthetic transformations, including the formation of more complex molecules.
- Synthetic Routes: The synthesis of this compound often involves multi-step organic reactions. The formation of isoquinoline is particularly of interest due to its various synthetic strategies, such as:
- Cyclization reactions
- Condensation reactions
- Electrophilic substitutions
- Research Potential: Due to the unique functionality of this compound, ongoing research may uncover new therapeutic avenues and applications in drug design. As quoted by chemist John R. Harris, "Every molecule holds a story, waiting to be uncovered."
In summary, 2-(2-chloroethyl)-3,4-dihydro-1H-isoquinoline not only exemplifies an important chemical structure but also serves as a reminder of the vast potential inherent in the world of organic compounds.