4-Chloroacetanilide
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- Molecular formula
- C8H8ClNO
- CAS Number
- 539-03-7
- IUPAC Name
- N-(4-chlorophenyl)-N-hydroxy-acetamide
- Molecular Weight
- 185.61g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3830g/cm3
- Synonyms
- N-(4-Chlorophenyl)-N-hydroxyacetamide
Identification
Interesting facts
Interesting Facts about N-(4-chlorophenyl)-N-hydroxy-acetamide
N-(4-chlorophenyl)-N-hydroxy-acetamide is a fascinating compound that unveils various intriguing aspects from its structure to its applications. Here are some noteworthy points:
- Chemical Structure: This compound features a chlorophenyl group, which is renowned for its influence on biological activity. The presence of the 4-chlorine substituent plays a crucial role in enhancing its efficacy.
- Pharmaceutical Relevance: N-(4-chlorophenyl)-N-hydroxy-acetamide has garnered attention for its potential applications in medicinal chemistry. Compounds containing the hydroxyamide functional group are often studied for their role in drug design, particularly in developing analgesics and anti-inflammatory agents.
- Mechanism of Action: The compound's hydroxyl group is pivotal in facilitating hydrogen bonding, which can significantly enhance its interaction with biological targets, such as enzymes and receptors.
- Research Potential: Scientists are continually investigating the biological properties of this compound. Studies have indicated that derivatives of N-(4-chlorophenyl)-N-hydroxy-acetamide can exhibit varying levels of antimicrobial activity, making it a candidate for further exploration.
- Safety and Toxicology: As with many chemical compounds, understanding the safety profile is essential. Preliminary studies often assess the toxicological aspects to ensure safe handling and application, especially for compounds with pharmaceutical implications.
In summary, N-(4-chlorophenyl)-N-hydroxy-acetamide is not just a simple compound; it's a potential cornerstone for advancements in medicinal chemistry, with its rich chemical characteristics opening avenues for research and development in various fields.