3,4-Dihydroisoquinolin-2-amine

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Identification

Molecular formula
C9H12N2
CAS Number
4542-46-3
IUPAC Name
3,4-dihydro-1H-isoquinolin-2-amine
Molecular Weight
146.21g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1373g/cm3
Synonyms
4836-98-0
Interesting facts

Interesting Facts about 3,4-Dihydro-1H-isoquinolin-2-amine

3,4-dihydro-1H-isoquinolin-2-amine is an intriguing organic compound that has captured the interest of researchers and chemists alike. This compound is particularly significant in the field of medicinal chemistry due to its potential biological activities. Here are some noteworthy aspects of this fascinating molecule:

  • Structural Uniqueness: The isoquinoline framework is quite unique, providing a rich platform for the synthesis of various derivatives. Its structure allows for interaction with biological targets in a manner that can lead to therapeutically relevant compounds.
  • Biological Applications: Compounds derived from isoquinoline have been studied for their roles in treating a range of conditions, including neurodegenerative diseases, cancer, and as anti-inflammatory agents. This makes 3,4-dihydro-1H-isoquinolin-2-amine a candidate for further research in pharmacology.
  • Synthetic Pathways: The synthesis of this compound often involves multi-step reactions, which can include cyclization and amination processes. Studying these pathways can provide insights into not only the compound itself but also the methodologies applicable to similar compounds.
  • Role in Natural Products: Isoquinoline derivatives are often found in various natural sources, such as plants. Understanding the biosynthesis of these compounds can lead to discoveries about their ecological roles and interactions.

As chemists continue to explore the broad implications of 3,4-dihydro-1H-isoquinolin-2-amine, they are likely to uncover more about its potential applications and benefits. The ongoing research in this area highlights the compound's importance in the continuous quest for new therapeutic agents.

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