Interesting facts
Interesting Facts About 2-bromo-N-methyl-N-(2,4,5-trichlorophenyl)acetamide
2-bromo-N-methyl-N-(2,4,5-trichlorophenyl)acetamide is a fascinating compound that belongs to the class of acetamides, renowned for its potential applications and biological activities. Here are some notable aspects of this compound:
- Biological Importance: This compound is of interest in medicinal chemistry for its potential as a pharmacological agent, particularly in studies related to anti-cancer activities due to its structural similarity to known antitumor agents.
- Substituent Effects: The presence of multiple chlorine atoms in the phenyl ring enhances the compound's reactivity and biological interactions. Chlorine substitution often influences the electronic properties and lipophilicity of aromatic compounds, making it a valuable area of study in drug design.
- Versatile Synthetic Pathways: Chemists have developed various synthetic strategies for creating compounds like this one, often involving reactions such as bromination and acylation. The synthetic pathways can illustrate key principles of organic chemistry, including nucleophilic substitution and electrophilic aromatic substitution.
- Research Applications: 2-bromo-N-methyl-N-(2,4,5-trichlorophenyl)acetamide is utilized in research to explore mechanisms of action in biological systems, specifically regarding its interaction with cellular targets and pathways.
- Environmental Impact: The presence of bromine and chlorine within its structure raises questions about its environmental fate and the implications of using halogenated compounds, emphasizing the importance of studies focused on environmental chemistry.
In conclusion, 2-bromo-N-methyl-N-(2,4,5-trichlorophenyl)acetamide serves as an important example of how organic compounds can hold vast potential for future applications while simultaneously posing challenges and questions about environmental and health impacts. As research continues, the full extent of its utility and effects will likely be unraveled.
Synonyms
23543-34-2
BRN 2127533
2-Bromo-N-methyl-2',4',5'-trichloroacetanilide
ACETANILIDE, 2-BROMO-N-METHYL-2',4',5'-TRICHLORO-
DTXSID40178131
RefChem:315740
DTXCID70100622
ACETANILIDE,2-BROMO-N-METHYL-2,4,5-TRICHLORO-
Solubility of 2-bromo-N-methyl-N-(2,4,5-trichlorophenyl)acetamide
The solubility of 2-bromo-N-methyl-N-(2,4,5-trichlorophenyl)acetamide can be quite interesting, given its complex structure.
Typically, the solubility of organic compounds like this one can be influenced by a variety of factors:
For 2-bromo-N-methyl-N-(2,4,5-trichlorophenyl)acetamide, one might expect moderate solubility in polar organic solvents, while its solubility in water could be limited due to the bulky, chlorinated aromatic substituents that dominate the molecular structure. These substituents can cause increased hydrophobic interactions, affecting its overall solubility profile.
In practical applications, knowledge of the solubility of this compound is crucial, as it will impact its bioavailability and effectiveness in various environments. Therefore, studying solubility can provide valuable insights into the compound's behavior and applications in chemical processes and formulations.