Neostigmine
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- Molecular formula
- C12H19N2O2
- CAS Number
- 59-99-4
- IUPAC Name
- trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium
- Molecular Weight
- 303.37g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3800g/cm3
- Synonyms
- 24474-85-9
Identification
Interesting facts
Interesting Facts About Trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium
Trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium is a fascinating compound that plays a significant role in various scientific fields, particularly in organic chemistry and biochemistry. Here are some intriguing points about this compound:
- Versatile Laboratory Applications: This compound is often utilized in laboratories as a reagent or intermediate in the synthesis of more complex molecules, making it valuable for chemists working on novel drug development.
- Biological Significance: The presence of the methylcarbamoyloxy group suggests potential biological activity. Compounds containing carbamates have been studied for their various biological properties, including antimicrobial and herbicidal activities.
- Ionization Properties: The trimethylammonium moiety in this compound contributes to its behavior as a quaternary ammonium salt, which can significantly influence solubility and ionization in polar media. This can enhance its reactivity in different chemical reactions.
- Structure-Activity Relationship: Researchers often examine how structural variations in compounds like trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium can affect their biological activity. This makes it a pivotal point of interest in medicinal chemistry.
- Potential for Drug Development: The exploration of compounds with similar structures has led to advancements in pharmaceuticals. Understanding this compound’s reactivity and interactions could pave the way for innovative therapeutic agents.
In summary, trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium is not just another chemical compound; it holds potential in organic synthesis and medicinal chemistry, showcasing the intricate relationship between structure, reactivity, and biological activity.