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3,3-diallyl-1-phenylindolin-2-one

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Identification
Molecular formula
C19H19NO
CAS number
3096-53-3
IUPAC name
3,3-diallyl-1-phenyl-indolin-2-one
State
State

At room temperature, 3,3-diallyl-1-phenyl-indolin-2-one is typically found in a solid state, often as crystalline powder.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
425.00
Boiling point (Kelvin)
698.15
General information
Molecular weight
285.36g/mol
Molar mass
285.3560g/mol
Density
1.1000g/cm3
Appearence

3,3-Diallyl-1-phenyl-indolin-2-one typically forms crystals or crystalline powder. The exact appearance can vary from off-white to slightly yellow, depending on purity and exposure to environmental factors such as light and air.

Comment on solubility

Solubility of 3,3-Diallyl-1-phenyl-indolin-2-one

The solubility of 3,3-diallyl-1-phenyl-indolin-2-one can vary significantly based on its molecular structure and the conditions under which it is tested. Here are some key points to consider:

  • Type of Solvent: This compound is likely to exhibit better solubility in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO) due to its non-polar and slightly polar characteristics.
  • Temperature: Increased temperature generally enhances solubility; thus, heating can improve the dissolution of 3,3-diallyl-1-phenyl-indolin-2-one in suitable solvents.
  • pH Levels: The solubility of this compound may be pH-dependent, where certain pH levels can lead to ionization, affecting its solubility.

In summary, while specific solubility data for 3,3-diallyl-1-phenyl-indolin-2-one might not be abundantly available, considering its structural attributes can provide insight into its potential solubility profiles. As always, experimental confirmation in various solvents under controlled conditions is recommended for precise information.

Interesting facts

Interesting Facts about 3,3-Diallyl-1-phenyl-indolin-2-one

3,3-Diallyl-1-phenyl-indolin-2-one is a fascinating compound that showcases the intricate world of organic chemistry. This compound belongs to the class of indole derivatives, which are known for their wide range of biological activities and applications in various fields.

Key Highlights:

  • Biological Significance: Indole derivatives, including 3,3-diallyl-1-phenyl-indolin-2-one, often exhibit significant pharmacological properties such as anti-inflammatory, antioxidant, and anti-cancer effects. This makes them valuable in medicinal chemistry.
  • Synthetic Versatility: The compound can be synthesized through several innovative pathways, allowing chemists to explore new methods of production while also creating variations with different functional groups.
  • Fluorescence: Certain indole derivatives can exhibit interesting photophysical properties, including fluorescence, which opens up avenues for their application in fluorescent probes and imaging techniques.
  • Research Applications: Its distinctive structure allows researchers to employ this compound in various chemical reactions, making it a potential subject for developing new catalysts or materials.

Overall, 3,3-diallyl-1-phenyl-indolin-2-one is not only a compound of theoretical interest but also a practical tool for advancing our understanding of chemical reactivity and biological interactions. As chemists continue to investigate its properties, further innovative uses are likely to emerge, indicating the compound's ongoing relevance in modern scientific research.

Synonyms
3,3-Diallyl-1-phenyl-2-indolinone
N-Phenyl-3,3-diallyloxoindole
2-INDOLINONE, 3,3-DIALLYL-1-PHENYL-
19048-20-5
BRN 1473729
DTXSID30172527
5-21-08-00517 (Beilstein Handbook Reference)
DTXCID3095018
3,3-Diallyl-1-phenylindolin-2-one