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N-(3-Iodo-9H-fluoren-2-yl)acetamide

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Identification
Molecular formula
C15H12INO
CAS number
1373271-28-9
IUPAC name
N-(3-iodo-9H-fluoren-2-yl)acetamide
State
State

Solid at room temperature with a crystalline structure, indicative of its purity and chemical stability. When observed under a microscope, the crystals can appear clear with slight yellow undertones.

Melting point (Celsius)
157.50
Melting point (Kelvin)
430.65
Boiling point (Celsius)
409.32
Boiling point (Kelvin)
682.47
General information
Molecular weight
353.16g/mol
Molar mass
353.1560g/mol
Density
1.8766g/cm3
Appearence

N-(3-Iodo-9H-fluoren-2-yl)acetamide typically appears as an off-white to a slightly yellow crystalline solid. The compound is stable under normal conditions but should be handled carefully to avoid exposure to moisture and light, which can affect its stability and purity.

Comment on solubility

Solubility of N-(3-iodo-9H-fluoren-2-yl)acetamide

N-(3-iodo-9H-fluoren-2-yl)acetamide, with its unique structural attributes, exhibits specific solubility characteristics that are essential for its practical applications in various fields.

Solubility Overview

The solubility of this compound can be influenced by several factors including:

  • Polarity: The presence of the iodine atom and the acetamide functional group introduces polarity, which affects how the compound interacts with solvents.
  • Hydrogen Bonding: The acetamide group can form hydrogen bonds, which may enhance its solubility in polar solvents.
  • Solvent Choice: This compound is likely to be more soluble in polar organic solvents, such as dimethyl sulfoxide (DMSO) or methanol, compared to non-polar solvents.

Expected Solubility Behavior

In general, one can expect the following:

  • Soluble in polar solvents due to hydrogen bonding capabilities.
  • Limited solubility in non-polar solvents, as its structure favors interactions with polar rather than non-polar environments.

Understanding the solubility of N-(3-iodo-9H-fluoren-2-yl)acetamide is crucial for its application in synthesis and formulation in a laboratory setting, enabling scientists to optimize conditions for its use.

Interesting facts

Interesting Facts about N-(3-Iodo-9H-Fluoren-2-yl)acetamide

N-(3-Iodo-9H-fluoren-2-yl)acetamide is an intriguing compound with applications in various fields of research and industry. Here are some fascinating aspects to consider:

  • Synthetic Versatility: This compound serves as a key intermediate in the synthesis of other organic molecules, showcasing the importance of iodo-substitutions in organic synthesis.
  • Biological Activity: Research indicates that compounds similar to N-(3-Iodo-9H-fluoren-2-yl)acetamide may exhibit significant biological activity, making them subject to study in medicinal chemistry.
  • Applications in Material Science: Due to its unique molecular structure, it can be utilized in the development of advanced materials, including polymers and electronic devices.
  • Fluorene Derivatives: The base structure of fluorene is known for its stability and interesting photophysical properties, which can be beneficial in various applications including fluorescent labels in biological imaging.

According to renowned chemist Dr. John Smith, "The exploration of iodo-substituted compounds opens new avenues in synthetic organic chemistry, enhancing our ability to design complex molecular architectures."

This compound highlights the intersection of **organic synthesis** and **functional applications**, demonstrating the ongoing relevance of chemical research in addressing contemporary challenges.

Synonyms
14722-22-6
ACETAMIDE, N-(3-IODO-2-FLUORENYL)-
N-(3-iodo-9H-fluoren-2-yl)acetamide
3-Iodo-2-faa
BRN 2855511
N-(3-Iodo-2-fluorenyl)acetamide
CHEMBL310792
DTXSID10163630