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Bromoindole-coumarin

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Identification
Molecular formula
C20H14BrN3O2
CAS number
420831-40-9
IUPAC name
N-[2-(6-bromo-1H-indol-3-yl)vinyl]-2-(1H-indol-3-yl)-2-oxo-acetamide
State
State

The compound exists as a solid under standard conditions of temperature and pressure.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
453.29g/mol
Molar mass
453.2900g/mol
Density
0.0000g/cm3
Appearence

The compound is typically a crystalline solid that can vary in color, often appearing as light brown to yellowish.

Comment on solubility

Solubility of N-[2-(6-bromo-1H-indol-3-yl)vinyl]-2-(1H-indol-3-yl)-2-oxo-acetamide (C20H14BrN3O2)

The solubility of a compound is a crucial property that can affect its biological activity, chemical behavior, and usability in various applications. For N-[2-(6-bromo-1H-indol-3-yl)vinyl]-2-(1H-indol-3-yl)-2-oxo-acetamide, the following points can be considered regarding its solubility:

  • Polarity: This compound contains multiple polar functional groups, which may increase its affinity for polar solvents like water.
  • Hydrophobic Interactions: The presence of indole rings may introduce some hydrophobic characteristics, potentially decreasing solubility in polar solvents.
  • Temperature Dependence: As with many organic compounds, solubility can be temperature-dependent. Elevated temperatures may enhance solubility.
  • pH Influence: Depending on the pH of the solution, ionizable groups can alter solubility, thus enhancing or reducing dissolution in aqueous media.

In summary, while it's not straightforward to determine the precise solubility behavior of N-[2-(6-bromo-1H-indol-3-yl)vinyl]-2-(1H-indol-3-yl)-2-oxo-acetamide without experimental data, understanding its structural features provides insight into its potential solubility characteristics. The compound may demonstrate varying solubility profiles in different solvents, influenced by several factors such as polarity, temperature, and pH. Experimentation under controlled conditions would yield the most definitive insights.

Interesting facts

N-[2-(6-bromo-1H-indol-3-yl)vinyl]-2-(1H-indol-3-yl)-2-oxo-acetamide

This fascinating compound, known as N-[2-(6-bromo-1H-indol-3-yl)vinyl]-2-(1H-indol-3-yl)-2-oxo-acetamide, is part of the indole family, characterized by its unique structure featuring an indol-3-yl ring. Here are some interesting insights into this compound:

  • Pharmacological Potential: Compounds with indole structures are known for their diverse biological activities, including anti-cancer, anti-inflammatory, and anti-viral properties. This specific compound might show promise in pharmaceutical applications due to its complex structure.
  • Brominated Variants: The presence of bromine in its structure can greatly influence the physical and chemical properties of the compound. Bromination often enhances biological activity, making brominated indoles a significant focus of research.
  • Synthetic Pathways: The synthesis of such compounds often involves multi-step reactions which can include carbon-carbon bond formation, making it a topic of interest in the field of organic chemistry. Understanding these pathways helps chemists design more efficient synthesis methods.
  • Research Applications: Researchers are continuously exploring the utility of indole derivatives in medicinal chemistry, expanding the therapeutic toolbox available for treating various ailments.

Overall, compounds like N-[2-(6-bromo-1H-indol-3-yl)vinyl]-2-(1H-indol-3-yl)-2-oxo-acetamide not only offer intriguing challenges in terms of synthesis and characterization but also pave the way for exciting developments in drug discovery and design.