Skip to main content

Clozapine

ADVERTISEMENT
Identification
Molecular formula
C18H19ClN4
CAS number
5786-21-0
IUPAC name
8-chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[b][1,4]benzodiazepine
State
State

At room temperature, clozapine is in a solid state, specifically as a crystalline powder.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
557.80
Boiling point (Kelvin)
830.95
General information
Molecular weight
326.83g/mol
Molar mass
326.8220g/mol
Density
1.2700g/cm3
Appearence

Clozapine typically appears as a pale, yellow, crystalline powder.

Comment on solubility

Solubility of 8-chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[1,4]benzodiazepine

The solubility of 8-chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[1,4]benzodiazepine is a critical aspect for its practical applications, particularly in pharmaceutical formulations. Generally speaking, the solubility of organic compounds, especially those containing complex structures such as this benzodiazepine derivative, can be influenced by several factors:

  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents.
  • Hydrogen bonding: Capability of forming hydrogen bonds often increases solubility in aqueous solutions.
  • Temperature: Solubility typically increases with temperature; thus, measuring at different temperatures can provide valuable information.
  • pH of the solution: For compounds with acidic or basic functional groups, pH can significantly affect their solubility.

For this specific compound, it's important to note that its solubility profile may vary greatly depending on the solvent used. As a guideline:

  1. In organic solvents such as DMSO or methanol, it may demonstrate moderate solubility based on its structure.
  2. In water, the solubility could be relatively low owing to its lipophilic character.
  3. The presence of the methylpiperazine group may also alter the compound's ability to interact with solvent molecules.

Overall, understanding the solubility of 8-chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[1,4]benzodiazepine is crucial for its utilization in biological systems and its effective incorporation into drug formulations. Each characteristic must be explored through empirical methods to draw accurate conclusions regarding its solubility behavior.

Interesting facts

Interesting Facts about 8-Chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[b][1,4]benzodiazepine

8-Chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[b][1,4]benzodiazepine is an intriguing compound that belongs to the class of benzodiazepines, known for their significant pharmacological properties. Here are some captivating insights about this compound:

  • Pharmacological Importance: This compound exhibits remarkable activity as a central nervous system (CNS) depressant. It is believed to have anxiolytic, sedative, and anticonvulsant effects, making it a potential candidate for various therapeutic applications.
  • Structural Features: The incorporation of both chlorine and piperazine groups into its structure contributes to its unique binding affinity to GABAA receptors. The presence of the piperazinyl moiety enhances the compound's effectiveness compared to other benzodiazepines.
  • Research Potential: Researchers are exploring this compound for its possible role in treating anxiety disorders and other related conditions. Its structural resemblance to existing benzodiazepines leads scientists to predict a variety of pharmacological effects.
  • Mechanism of Action: Like many benzodiazepines, it is believed to enhance the effects of the neurotransmitter gamma-aminobutyric acid (GABA), leading to increased inhibitory transmission in the CNS. This mechanism is crucial for its therapeutic effects.
  • Chemistry and Synthesis: The synthesis of this compound involves intricate organic reactions, highlighting the importance of synthetic organic chemistry in drug development. Understanding its synthesis can lead to innovations in creating novel compounds with enhanced properties.

As the study of benzodiazepines continues to expand, 8-chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[b][1,4]benzodiazepine stands out as a compound worth investigating due to its potential implications in therapeutic applications and the remarkable chemistry behind its formation.

Synonyms
ISOCLOZAPINE
2-Chloro-11-(4-methyl-1-piperazinyl)-5H-dibenzo(b,e)(1,4)diazepine
1977-08-8
4Q6V732VRT
CHEMBL415300
8-chloro-6-(4-methylpiperazin-1-yl)-11H-benzo[b][1,4]benzodiazepine
2-Chloro-11-(4-methyl-piperazin-1-yl)-5H-dibenzo[b,e][1,4]diazepine
5H-DIBENZO(b,e)(1,4)DIAZEPINE, 2-CHLORO-11-(4-METHYL-1-PIPERAZINYL)-
BRN 0763655
UNII-4Q6V732VRT
SCHEMBL140207
DTXSID40173464
BAA97708
2-Chloro-11-(4-methyl-1-piperazinyl)-5H-benzo(b,e)(1,4)diazepine
BDBM50010594
NCGC00386501-01
DB-217114
E98703
2-Chloro-11-(4-methyl-piperazin-1-yl)-5H-dibenzo[b,e][1,4]diazepine(isoclozapine)
8-CHLORANYL-6-(4-METHYLPIPERAZIN-1-YL)-11H-BENZO(B)(1,4)BENZODIAZEPINE