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2-iodo-N-(3-methoxyphenyl)acetamide

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Identification
Molecular formula
C9H10INO2
CAS number
65200-06-6
IUPAC name
2-iodo-N-(3-methoxyphenyl)acetamide
State
State

Solid at room temperature. It is typically encountered as a powdery or crystalline substance.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.15
Boiling point (Celsius)
329.40
Boiling point (Kelvin)
602.55
General information
Molecular weight
277.09g/mol
Molar mass
277.0680g/mol
Density
1.8290g/cm3
Appearence

2-Iodo-N-(3-methoxyphenyl)acetamide typically appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of 2-iodo-N-(3-methoxyphenyl)acetamide

2-iodo-N-(3-methoxyphenyl)acetamide is characterized by its unique solubility properties, which are influenced by both its molecular structure and functional groups. Understanding the solubility of this compound is crucial for applications in various chemical processes.

Below are some key points regarding its solubility:

  • Polar vs. Nonpolar: The presence of the 3-methoxyphenyl group introduces a polar character, enhancing solubility in polar solvents like water.
  • Solvent Dependence: It tends to have better solubility in organic solvents such as ethanol and methanol due to the hydrophobic character of the aromatic ring.
  • Temperature Effects: An increase in temperature typically increases the solubility of solids; thus, heating can often facilitate the dissolution of this compound in various solvents.
  • Functional Group Influence: The amide functional group can engage in hydrogen bonding, which can further affect solubility in polar environments.

In conclusion, the solubility behavior of 2-iodo-N-(3-methoxyphenyl)acetamide presents a fascinating interplay of molecular interactions and solvent characteristics. As one can observe, its solubility is predominantly governed by the balance of polar and nonpolar interactions, making solvent choice critical in practical applications.

Interesting facts

Exploring 2-Iodo-N-(3-Methoxyphenyl)acetamide

2-Iodo-N-(3-methoxyphenyl)acetamide is an intriguing compound that has captured the attention of chemists for several reasons. As an aromatic amide derivative, it exhibits both structural complexity and potential utility in various applications.

Key Features of 2-Iodo-N-(3-methoxyphenyl)acetamide

  • Functional Groups: This compound contains both an iodine substituent and an acetamide functional group, making it a versatile molecule for further chemical reactions.
  • Biological Significance: Compounds containing iodine are often studied for their biological properties, including antibacterial and antifungal activities. The presence of the methoxy group may enhance the compound's interaction with biological systems.
  • Synthetic Applications: As a reactant or intermediate, it can be used to synthesize more complex molecules in medicinal chemistry. This is particularly valuable in the development of pharmaceuticals.
  • Research Potential: The unique structure of this compound makes it a subject of interest in studying structure-activity relationships (SAR) in drug design.

Furthermore, researchers have noted that compounds like 2-iodo-N-(3-methoxyphenyl)acetamide can serve as critical links in the synthesis of new materials and therapeutic agents. Innovative studies could uncover additional properties or uses that may not yet be widely recognized, paving the way for future discoveries in the field of chemistry.

In summary, 2-iodo-N-(3-methoxyphenyl)acetamide is more than just a chemical compound; it embodies a blend of structural beauty and scientific potential, making it a noteworthy example for students and professionals alike.

Synonyms
2-iodo-N-(3-methoxyphenyl)acetamide
17641-09-7
m-ACETANISIDIDE, 2-IODO-
2-Iodo-m-acetanisidide
N-(Iodoacetyl)-m-anisidide
BRN 2720729
starbld0036899
orb1985741
SCHEMBL3753125
DTXSID40170130
AKOS014116549