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Methyl 3-acetamido-5-(acetamidomethyl)-2,4,6-triiodobenzoate

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Identification
Molecular formula
C15H15I3N2O4
CAS number
1992-08-3
IUPAC name
methyl 3-acetamido-5-(acetamidomethyl)-2,4,6-triiodo-benzoate
State
State

The compound is typically a solid at room temperature due to its crystalline nature and high molecular weight.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
378.00
Boiling point (Kelvin)
651.15
General information
Molecular weight
665.05g/mol
Molar mass
665.0450g/mol
Density
2.1100g/cm3
Appearence

Methyl 3-acetamido-5-(acetamidomethyl)-2,4,6-triiodobenzoate is typically found as a white or almost white crystalline powder. It is used as an intermediate in the synthesis of more complex compounds, often characterized by its crystalline structure.

Comment on solubility

Solubility of Methyl 3-Acetamido-5-(Acetamidomethyl)-2,4,6-triiodo-benzoate

The solubility of methyl 3-acetamido-5-(acetamidomethyl)-2,4,6-triiodo-benzoate can be influenced by several key factors due to its unique structure and functional groups.

  • Polarity: The presence of multiple acetamido groups can increase the polarity of the molecule, potentially enhancing its solubility in polar solvents such as water.
  • Hydrophobic Interactions: The triiodo substitution introduces hydrophobic characteristics that may decrease solubility in non-polar solvents.
  • Temperature Dependency: Solubility can vary with temperature; typically, increased temperature can lead to increased solubility for many compounds.
  • pH Sensitivity: Since the compound contains amide functional groups, its solubility might also be affected by the pH of the solution.

In summary, while specific solubility data for this compound may not be widely available, understanding these factors can provide insights into its potential behavior in various solvents. As a rule of thumb, “like dissolves like” is a fundamental principle to consider when predicting solubility outcomes.

Interesting facts

Interesting Facts about Methyl 3-Acetamido-5-(Acetamidomethyl)-2,4,6-Trijodo-Benzoate

Methyl 3-acetamido-5-(acetamidomethyl)-2,4,6-triiodo-benzoate is a unique compound that showcases the fascinating intersection of organic chemistry and medicinal applications. Here are some engaging aspects of this compound:

  • Structure and Complexity: With multiple functional groups and iodine atoms incorporated into its structure, this compound highlights the complexity that can arise from judicious functionalization in organic synthesis.
  • Biological Activity: Triiodophenolic derivatives have been widely studied for their biological activity, particularly in areas such as antimicrobial and anti-cancer investigations. The presence of iodine enhances their reactivity and potential therapeutic effects.
  • Versatile Applications: This compound can serve as a key intermediate in the synthesis of other valuable pharmaceutical agents, illustrating the importance of understanding structure-activity relationships in drug discovery.
  • Research and Development: Due to its intricate molecular framework, it provides ample opportunity for research in areas such as medicinal chemistry, biochemistry, and organic synthesis. It enables scientists to explore novel mechanisms of action through its diverse functional groups.
  • Environmental Impact: While using iodine in compounds can raise concerns regarding environmental persistence, understanding and mitigating these effects is crucial as we develop new materials to ensure safety and sustainability.

This compound exemplifies the challenges and rewards of working with complex organic molecules. Through its unique properties, researchers can unlock new avenues for innovation in pharmaceutical development, highlighting the ever-evolving nature of chemical science.

Synonyms
BRN 2776128
B 15570
BENZOIC ACID, 3-ACETAMIDO-5-ACETAMIDOMETHYL-2,4,6-TRIIODO-, METHYL ESTER
739-52-6
DTXSID10224477
3-Acetamido-5-acetamidomethyl-2,4,6-triiodobenzoic acid methyl ester
DTXCID10146968