Lobeline hydrochloride
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- Molecular formula
- C12H21NO2
- CAS Number
- 134-63-4
- IUPAC Name
- 5-(1,1-dimethylpentyl)-7-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-6-ium;chloride
- Molecular Weight
- 475.08g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0900g/cm3
- Synonyms
- 20233-00-5
Identification
Interesting facts
Interesting Facts about 5-(1,1-dimethylpentyl)-7-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-6-ium; chloride
This compound is a fascinating member of the isoquinoline family, showcasing the complexity and diversity of chemical structure within organic compounds. Here are some noteworthy aspects:
- Multi-faceted Structure: The compound features a unique [1,3]dioxolo ring fused with an isoquinoline core, which is married with a quaternary ammonium structure. This combination makes it intriguing for researchers interested in the interplay of aromatic and aliphatic characteristics.
- Potential Biological Relevance: Many isoquinoline derivatives are known for their broad range of biological activities. Studying this compound may lead to insights or applications in drug discovery, particularly in developing therapeutics that harness its chemical properties.
- Versatile Applications: The structural complexity of this compound poses interesting prospects in fields such as organic synthesis and material science. It can be explored for uses in dyes, sensors, or even in improving the efficiency of light-emitting diodes (LEDs).
- Research Implications: The presence of a dimethylpentyl group suggests enhanced lipophilicity, possibly affecting the compound's bioavailability or interaction with biological targets, making it a valuable subject for further investigation.
- Chloride Role: Being paired with chloride as a counter ion may provide clues into its solubility and ionic interactions, aspects critical to its function in biological systems.
This compound exemplifies how intricate chemical structures can lead to diverse applications and mechanisms of action, stimulating curiosity within both chemistry and biological communities.