Propoxur
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- Molecular formula
- C11H15Cl2NO3
- CAS Number
- 114-26-1
- IUPAC Name
- 2-(1-piperidyl)ethyl N-(2,6-dichloro-4-propoxy-phenyl)carbamate
- Molecular Weight
- 251.16g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2700g/cm3
- Synonyms
- K 922
Identification
Interesting facts
Interesting Facts about 2-(1-Piperidyl)ethyl N-(2,6-dichloro-4-propoxy-phenyl)carbamate
This compound is notable for its intriguing structure and potential applications in various fields of chemistry and pharmacology. Here are some fascinating details:
- Pharmacological Potential: The presence of the piperidine ring suggests that this compound may interact with neurotransmitter systems, particularly in the central nervous system. Compounds with similar structures are often investigated as potential therapeutic agents in treating neurological disorders.
- Chlorine Atoms: The inclusion of dichloro groups in the molecular structure can significantly enhance the compound's reactivity and efficacy, making it a subject of interest when studying how halogen substitutions can optimize biological activity.
- Carbamate Derivative: As a carbamate, this compound could exhibit insecticidal or herbicidal properties, as many carbamate derivatives have been employed in agriculture for pest control.
- Structure-Activity Relationship (SAR): This compound serves as an excellent model for exploring SAR, which examines how variations in chemical structure can influence biological activity. By altering the alkyl groups or substituents, researchers can determine which modifications yield the best pharmacological effects.
- Research Applications: Its unique composition makes this compound valuable for research in medicinal chemistry, where scientists aim to develop new drugs that mimic natural biological processes.
As scientists continue to investigate the potential of compounds like 2-(1-piperidyl)ethyl N-(2,6-dichloro-4-propoxy-phenyl)carbamate, they uncover new possibilities for therapeutic applications and advancements in chemical synthesis.