5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide
- Molecular formula
- C13H8Cl2N2O4
- CAS Number
- 69579-82-4
- IUPAC Name
- 5-chloro-N-(2-chloro-4-nitro-phenyl)-2-hydroxy-benzamide
- Molecular Weight
- 330.11g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5200g/cm3
- Synonyms
- niclosamide
Identification
Interesting Facts about 5-chloro-N-(2-chloro-4-nitro-phenyl)-2-hydroxy-benzamide
This compound, commonly known in the realm of organic chemistry and pharmacology, is a fascinating example of a halogenated aromatic amide. It showcases intricate structural features due to the presence of both chlorine and nitro substituents, which significantly influence its chemical behavior and biological activity.
Chemical Versatility
- Reactivity: The presence of chlorine and nitro groups can enhance the compound's reactivity, making it suitable for various chemical transformations.
- Biological Activity: Compounds with similar structures are often investigated for their potential as pharmaceutical agents, given their ability to interact with biological targets.
Applications in Research
This compound serves as a valuable intermediate in the synthesis of more complex molecules. Researchers often explore its utility in:
- Synthesizing dyes and pigments.
- Studying interactions in biological systems, particularly in drug development.
Safety Considerations
While engaging with this compound, safety is paramount. Halogenated compounds can exhibit:
- Toxicity: Some halogenated aromatic compounds can be hazardous and require careful handling and disposal practices.
- Environmental Impact: The environmental persistence of similar compounds necessitates exploring greener alternatives or mitigation strategies during chemical synthesis.
Research Opportunities
The study of 5-chloro-N-(2-chloro-4-nitro-phenyl)-2-hydroxy-benzamide can pave the way for novel discoveries:
- Investigating structure-activity relationships (SAR) for potential drug candidates.
- Understanding mechanisms of action within specific biological pathways.
In summary, 5-chloro-N-(2-chloro-4-nitro-phenyl)-2-hydroxy-benzamide presents numerous avenues for exploration in chemical synthesis, pharmacology, and environmental sciences. Its unique structure and potential applications continue to captivate scientists in their quest for new knowledge.