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2-Iodo-N-(4-methoxyphenyl)acetamide

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Identification
Molecular formula
C9H10INO2
CAS number
14829-00-4
IUPAC name
2-iodo-N-(4-methoxyphenyl)acetamide
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
131.50
Melting point (Kelvin)
404.65
Boiling point (Celsius)
342.20
Boiling point (Kelvin)
615.35
General information
Molecular weight
291.09g/mol
Molar mass
291.0770g/mol
Density
2.0360g/cm3
Appearence

2-Iodo-N-(4-methoxyphenyl)acetamide appears as a solid. The exact color and crystal structure may vary and it typically requires specification from experimental observation. Most compounds in this class are either colorless or pale yellow-brown depending on purity and light exposure.

Comment on solubility

Solubility of 2-iodo-N-(4-methoxyphenyl)acetamide

The compound 2-iodo-N-(4-methoxyphenyl)acetamide is known for its interesting solubility profile which is influenced by both its structure and the presence of functional groups.

Generally, solubility can be categorized as:

  • Water Solubility: This compound is expected to have limited solubility in water due to its organic nature and the presence of the iodo group, which can hinder hydrogen bonding.
  • Organic Solvents: However, it tends to be more soluble in organic solvents such as ethanol, acetone, or dichloromethane. This is attributed to the nonpolar characteristics of the methoxy and iodine substituents.

In summary, we can say:

"Solubility is contingent upon the balance between hydrophilic and hydrophobic interactions."

Recognizing the interplay of these forces gives insight into why 2-iodo-N-(4-methoxyphenyl)acetamide exhibits selective solubility in specific solvents rather than broadly in aqueous environments. Its unique combination of functional groups provides a rich landscape for further exploration of its solubility properties.

Interesting facts

Interesting Facts about 2-Iodo-N-(4-methoxyphenyl)acetamide

2-Iodo-N-(4-methoxyphenyl)acetamide is a fascinating compound that captures the interest of chemists due to its unique structure and potential applications. Here are some intriguing aspects of this compound:

  • Structural Diversity: The presence of both the iodine atom and the methoxy group introduces significant steric and electronic effects, making the compound a noteworthy example of molecular design.
  • Biological Significance: Compounds of this nature, particularly those with halogens and aromatic rings, often exhibit interesting biological properties, making them candidates for drug development and medicinal chemistry.
  • Reaction Chemistry: The iodo substituent can participate in numerous substitution reactions, offering a versatile route for further functionalization of the compound.
  • Applications in Research: Due to its structure, 2-iodo-N-(4-methoxyphenyl)acetamide can be utilized in synthetic organic chemistry for the development of new materials or in the study of chemical reactivity.

As we continue to explore the potential of such compounds, it is important to note the words of the famous chemist Linus Pauling: “The best way to have a good idea is to have lots of ideas.” This statement certainly is applicable in the realm of organic synthesis, where variations in molecular structure open doors to endless possibilities in research and application.

Overall, 2-iodo-N-(4-methoxyphenyl)acetamide stands as an excellent representative of how modifying a compound's structure can lead to unique properties and applications, reinforcing the concept of creativity and innovation in the field of chemistry.

Synonyms
p-ACETANISIDIDE, 2-IODO-
19303-11-8
2-Iodo-p-acetanisidide
N-(Iodoacetyl)-p-anisidide
BRN 2967550
DTXSID50172908
AKOS014115900