granisetron hydrochloride
- Molecular formula
- C18H24Cl2N4
- CAS Number
- 107007-99-8
- IUPAC Name
- (3-azaniumyl-4-pyridyl)-[2-(1H-indol-3-yl)ethyl]ammonium;dichloride
- Molecular Weight
- 312.87g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3700g/cm3
Identification
Interesting Facts about (3-azaniumyl-4-pyridyl)-[2-(1H-indol-3-yl)ethyl]ammonium;dichloride
This intriguing compound, often referred to in the scientific community for its unique structural features, showcases a fascinating combination of organic functional groups that contribute to its potential applications in various fields. Here are a few compelling aspects:
- Complex Structure: The compound is derived from an indole core, which is a structure frequently found in many biologically active molecules, including neurotransmitters and pharmaceuticals. This highlights its possible significance in medicinal chemistry.
- Dichloride Salt: As a salt, the dichloride form can enhance its solubility and stability, making it a useful candidate for experimental studies and potential drug formulations.
- Biological Activity: Compounds with indole moieties are known for their diverse biological activities, including anti-cancer, anti-inflammatory, and antimicrobial properties, opening the door for research on new therapeutic agents.
- Rotational Flexibility: The ethyl bridge connecting the indole and pyridine structures may introduce a degree of rotational flexibility. This could impact the compound's interaction with biological targets and affect its efficacy.
- Potential Applications: Given its unique properties, this compound could be explored for applications in drug design, synthetic chemistry, and materials science. It might serve as a precursor for creating more complex molecules.
Chemists are always excited about compounds like this, which not only illustrate the elegance of molecular architecture but also hold the promise of contributing significantly to advancements in health and materials technology. The interplay of the azaniumyl and pyridyl groups in this compound further invites a closer look to decipher its interaction mechanisms and effects.