Acetanisole

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Identification

Molecular formula
C9H10O2
CAS Number
100-06-1
IUPAC Name
N-(4-methoxyphenyl)acetamide
Molecular Weight
151.17g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1430g/cm3
Synonyms
N-(4-Methoxyphenyl)acetamide
Interesting facts

Exciting Facts about N-(4-methoxyphenyl)acetamide

N-(4-methoxyphenyl)acetamide, often referred to as a derivative of acetanilide, presents a captivating profile in the realm of organic chemistry. Here are some intriguing aspects to consider:

  • Structural Significance: The presence of the 4-methoxyphenyl group significantly influences the compound's reactivity and properties. This substitution can enhance biological activity, thus making it an important candidate in pharmaceutical research.
  • Versatile Applications: Due to its structure, N-(4-methoxyphenyl)acetamide may find a variety of applications in medicinal chemistry. It is often studied for its potential use as an analgesic or anti-inflammatory agent.
  • Intriguing Mechanisms: The interaction between the methoxy group and the aromatic ring plays a crucial role in how this compound interacts with enzymes and receptors, making it a subject of interest in drug design.
  • Synthetic Pathways: Chemists often explore different synthetic methods to produce this compound, including the use of acylation reactions that showcase its versatility and adaptability in laboratory settings.
  • Study of Substituent Effects: The compound serves as an excellent model for studying how different substituents impact the electronic properties of phenyl rings, an essential concept in organic chemistry.

As you dive into the properties and uses of N-(4-methoxyphenyl)acetamide, consider the implications of its unique structure. Understanding such compounds not only enhances our knowledge of organic chemistry but also opens doors for innovative drug discovery and design.

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