Lorazepam acetate
- Molecular formula
- C17H11Cl2N2O4
- CAS Number
- 29177-30-8
- IUPAC Name
- [7-chloro-5-(2-chlorophenyl)-2-oxo-1,3-dihydro-1,4-benzodiazepin-3-yl] acetate
- Molecular Weight
- 408.18g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3940g/cm3
- Synonyms
- Lorazepam acetate
Identification
Interesting Facts About [7-chloro-5-(2-chlorophenyl)-2-oxo-1,3-dihydro-1,4-benzodiazepin-3-yl] Acetate
[7-chloro-5-(2-chlorophenyl)-2-oxo-1,3-dihydro-1,4-benzodiazepin-3-yl] acetate is a fascinating compound in the realm of medicinal chemistry, particularly within the context of the benzodiazepine class of drugs. Here are some intriguing aspects:
- Benzodiazepine Class: This compound shares the characteristic structure of benzodiazepines, which are renowned for their anxiolytic (anti-anxiety), sedative, and muscle relaxant properties. This structural similarity contributes significantly to its pharmacological effects.
- Chlorine Atoms: The presence of chlorine atoms in its structure not only enhances the compound’s biological activity but also influences its metabolic stability. Chlorinated compounds often exhibit improved potency and selectivity in their interactions with biological targets.
- Synthetic Applications: The synthesis of this compound is particularly noteworthy as it exemplifies the **application of organic synthesis skills** within medicinal chemistry. Researchers consistently explore the modifications of benzodiazepine derivatives to optimize their therapeutic effects.
- Potential Uses: Although primarily studied for its sedative effects, the broader range of benzodiazepines are also investigated for their utility in treating conditions such as insomnia, anxiety disorders, and seizure disorders. As such, compounds like this acetate may hold promise in various therapeutic applications.
- Research Significance: Scientists are motivated to explore this compound due to its potential **to lead to the development of new medications** with fewer side effects or improved efficacy, which is a significant consideration in pharmacology.
As with many benzodiazepine derivatives, understanding the mechanisms of action and interaction with gamma-aminobutyric acid (GABA) receptors is crucial for enhancing our knowledge of how this class of compounds can be effectively applied in clinical settings. The study of compounds like [7-chloro-5-(2-chlorophenyl)-2-oxo-1,3-dihydro-1,4-benzodiazepin-3-yl] acetate continually highlights the intricate balance of structure-activity relationships in drug design.