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3,3-bis(2-hydroxypropyl)-1-phenylindolin-2-one

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Identification
Molecular formula
C22H25NO3
CAS number
123312-89-0
IUPAC name
3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one
State
State

At room temperature, 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one is solid. It's relatively stable under standard conditions but can undergo transformations or decompositions under varying environmental factors.

Melting point (Celsius)
103.50
Melting point (Kelvin)
376.65
Boiling point (Celsius)
547.20
Boiling point (Kelvin)
820.35
General information
Molecular weight
339.45g/mol
Molar mass
339.4100g/mol
Density
1.2074g/cm3
Appearence

3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one typically appears as a solid crystalline substance. The color can vary slightly based on purity but often it is a light yellow or off-white.

Comment on solubility

Solubility of 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one

The solubility of 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one is an intriguing aspect to explore, particularly due to its unique molecular structure, which may influence its interactions with solvents. Here are some key points regarding its solubility:

  • Polarity Influence: The presence of hydroxyl (-OH) groups in the molecule increases polarity, which generally enhances solubility in polar solvents like water.
  • Hydroxyl Groups: These groups can form hydrogen bonds with water, promoting solubility. The more hydroxyl groups present, the greater the potential solubility in aqueous solutions.
  • Solvent Compatibility: In addition to water, 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one may exhibit significant solubility in organic solvents such as ethanol or methanol due to its organic nature.
  • Temperature Effects: As with many organic compounds, increased temperature can often lead to enhanced solubility, allowing better dissolution in a chosen solvent.

Overall, while specific solubility data may vary, the intricate balance of structural characteristics such as the number of hydroxyl groups and overall molecular polarity strongly influences the solubility characteristics of this compound. As the adage goes, "like dissolves like," and understanding these relationships can significantly aid in predicting solubility behavior.

Interesting facts

Interesting Facts about 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one

This compound is a fascinating member of the indolin family, known for its wide range of applications in various fields such as organic electronics, dye-sensitized solar cells, and medicinal chemistry. Here are some intriguing aspects of this particular compound:

  • Versatility in Application: The structure of 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one allows it to act both as a dye and a potential organic semiconductor. Its ability to absorb light makes it particularly interesting for applications in solar energy conversion.
  • Medicinal Potential: Compounds derived from indolin structures have been studied for their biological activities. Research indicates that this compound may exhibit anti-cancer properties, raising interest for further pharmacological studies.
  • Hydroxypropyl Groups: The presence of two hydroxypropyl groups contributes to its solubility and reactivity, making it easier to modify for specific applications. This functionalization is crucial in tuning the properties of the compound for desired behavior in chemical reactions.
  • Research Interest: Ongoing research focuses on the synthesis and modification of indolin derivatives to enhance their effectiveness as photovoltaic materials. Reports suggest that innovative approaches to blend these compounds with other nanomaterials can lead to improved efficiency.
  • Color Variety: As an organic compound, the color of 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one can vary considerably depending on its molecular interactions and the surrounding environment, making it a subject of interest in colorimetric sensing applications.

In conclusion, 3,3-bis(2-hydroxypropyl)-1-phenyl-indolin-2-one is not just a simple chemical compound; it is a versatile and promising substance that continues to pique the curiosity of chemists and researchers worldwide. Its dual role in both the medicinal and electronic realms showcases the interconnectedness of chemistry and innovation.

Synonyms
20870-64-8
3,3-Bis(2-hydroxypropyl)-1-phenylindolin-2-one
3,3-Bis(2-hydroxypropyl)-1-phenyl-2-indolinone
BRN 1593699
N-Phenyl-3,3-di(beta-hydroxypropyl)oxoindole
2-INDOLINONE, 3,3-BIS(2-HYDROXYPROPYL)-1-PHENYL-
DTXSID60943126
5-21-13-00109 (Beilstein Handbook Reference)
3,3-Bis(2-hydroxypropyl)-1-phenyl-1,3-dihydro-2H-indol-2-one