Interesting facts
Interesting Facts about N-(4-Chlorophenyl)benzohydrazonoyl Chloride
N-(4-Chlorophenyl)benzohydrazonoyl chloride, a compound with significant applications in various fields, stands out due to its chemical structure and reactivity. Here are some engaging insights:
- Versatile Intermediate: This compound serves as a valuable intermediate in the synthesis of numerous pharmaceuticals and agrochemicals, underscoring its utility in organic synthesis.
- Analytical Chemistry: It finds application in analytical chemistry as a reagent for the determination of certain chemical compounds. The specificity of its reactions can help in identifying target molecules.
- Therapeutic Potential: Research indicates that derivatives of this compound may exhibit potential therapeutic properties, making it a candidate of interest for drug development.
- Biological Activity: Some studies suggest that compounds similar to N-(4-chlorophenyl)benzohydrazonoyl chloride demonstrate anti-cancer activity, highlighting their importance in medicinal chemistry.
- Chlorine's Role: The presence of the chlorine atom in its structure can significantly influence its reactivity and biological activity, often enhancing the compound's lipophilicity and facilitating cellular absorption.
As we continue to explore the vast landscape of chemical compounds, N-(4-chlorophenyl)benzohydrazonoyl chloride exemplifies the intricate relationship between structure and function in chemistry. Its ongoing research and potential applications make it an exciting topic of investigation in both academic and industrial settings.
In the words of a renowned chemist, "The beauty of chemistry lies in the unseen potential of every compound, waiting to be unveiled through exploration."
Synonyms
17359-82-9
N-(4-Chlorophenyl)benzenecarbohydrazonoyl chloride
DTXSID701227428
Solubility of N-(4-chlorophenyl)benzohydrazonoyl chloride
N-(4-chlorophenyl)benzohydrazonoyl chloride is a unique compound known for its specific solubility characteristics. When evaluating the solubility of this compound, several factors come into play:
In conclusion, N-(4-chlorophenyl)benzohydrazonoyl chloride is more soluble in non-polar and slightly polar organic solvents, while exhibiting limited solubility in water. This selective solubility profile can be attributed to its molecular structure and the interactions between the solvent and solute, making it an interesting case in solubility studies.