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Indigo

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Identification
Molecular formula
C16H10N2O2
CAS number
482-89-3
IUPAC name
2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide
State
State
At room temperature, indigo is typically solid. It is usually found in powder or granule form due to its insolubility in water and is primarily used as a dye in various industries.
Melting point (Celsius)
390.00
Melting point (Kelvin)
663.00
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.00
General information
Molecular weight
262.27g/mol
Molar mass
262.2740g/mol
Density
1.4000g/cm3
Appearence

Indigo appears as dark blue crystals or granules, and can sometimes appear black. In its powdered form, it is less intense in color. It is a water-insoluble dye that has been used historically for dyeing fabrics a deep blue.

Comment on solubility

Solubility of 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide

The compound 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide, with the molecular formula C16H10N2O2, presents interesting characteristics regarding its solubility. Understanding the solubility of this compound is essential, as it impacts its applications in various fields such as pharmaceuticals and materials science.

Key Aspects of Solubility

This compound can generally be classified based on several key factors:

  • Polarity: The presence of polar functional groups (such as the acetamide moiety) suggests that the compound may exhibit some level of solubility in polar solvents like water and alcohols.
  • Hydrophobic Interactions: The indole rings are hydrophobic in nature, which can limit solubility in highly polar environments while improving solubility in organic solvents.
  • pH Sensitivity: The solubility may also be pH-dependent, as the presence of amide groups can lead to protonation or deprotonation depending on the surrounding conditions.

To summarize, one might find that:

  1. This compound is likely soluble in organic solvents (e.g., DMSO, ethanol).
  2. Its solubility in water may be moderate due to the balance of polar and non-polar components.
  3. Adjustments in temperature and pH could enhance its solubility characteristics.

In conclusion, the solubility of 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide is influenced by its unique molecular structure, making it a compound of interest for further studies in solubility behavior under varying conditions.

Interesting facts

Interesting Facts About 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide

The compound 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide exhibits fascinating properties and potential applications in scientific research. Here are some intriguing aspects of this compound:

  • Indole Framework: This compound features a unique indole structure, a bicyclic compound known for its presence in many natural products and pharmaceuticals. Indole derivatives have been recognized for their biological activities, including anticancer, anti-inflammatory, and antimicrobial properties.
  • Vinyl Group Influence: The presence of a vinyl group is significant as it can influence the compound's reactivity and stability. This structural motif can facilitate various chemical reactions and has implications for drug design and synthesis.
  • Potential in Drug Discovery: Due to its unique structure, this compound could serve as a promising candidate in the realm of drug discovery, especially in targeting specific biological pathways associated with diseases.
  • Chemical Versatility: The compound can undergo various transformations that make it suitable for implementing in synthetic organic chemistry, leading to diverse derivatives and analogs that may have enhanced activity or selectivity.
  • Research Interest: Researchers have expressed keen interest in exploring compounds with indole motifs for their potential use in treating complex diseases, encouraging ongoing studies in medicinal and organic chemistry.

In conclusion, 2-(1H-indol-3-yl)-N-[2-(1H-indol-3-yl)vinyl]-2-oxo-acetamide serves as a prime example of how chemical structure intertwines with biological function, supporting the continuous pursuit of new therapeutic agents in the field of medicinal chemistry.