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3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile

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Identification
Molecular formula
C19H13N2
CAS number
1227234-41-1
IUPAC name
3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile
State
State

At room temperature, 3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile is in a solid state. It is usually stable and can be handled safely in typical laboratory environments with proper personal protective equipment.

Melting point (Celsius)
107.50
Melting point (Kelvin)
380.65
Boiling point (Celsius)
379.30
Boiling point (Kelvin)
652.45
General information
Molecular weight
279.34g/mol
Molar mass
279.3350g/mol
Density
1.1597g/cm3
Appearence

3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile typically appears as a solid crystalline powder. The crystals can range in color from white to pale yellow, depending on the purity and specific conditions of crystallization.

Comment on solubility

Solubility of 3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile

The solubility of 3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile can be quite interesting, reflecting the complex interactions of its molecular structure. This compound, associated with a unique arrangement of functional groups, often exhibits characteristics that influence its solubility in various solvents.

Key points to consider regarding its solubility include:

  • Polarity: The presence of cyano (–C≡N) groups generally increases polarity, which can enhance solubility in polar solvents such as water and alcohols.
  • Solvent Compatibility: Non-polar solvents, like hexane or toluene, might show limited solubility due to the polar nature of the cyano group.
  • Temperature Influence: Temperature changes can play a significant role, potentially increasing solubility as kinetic energy allows for greater interaction between solute and solvent.

In summary, while solubility tends to align with the compound's polar characteristics, external factors such as solvent choice and temperature may greatly influence the extent to which 3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile dissolves. Understanding these dynamics is crucial for applications in research and industry.

Interesting facts

Interesting Facts about 3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile

3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile is a fascinating compound in the realm of organic chemistry, particularly due to its unique structure and potential applications. Here are some intriguing aspects:

  • Fluorene Derivative: This compound is a derivative of fluorene, characterized by a fused-ring structure that imparts interesting electronic properties. Its basic framework contributes to strong photophysical activities, making it suitable for studying photochemical reactions.
  • Cyanoethyl Group: The presence of a cyanoethyl group adds versatility to the compound. Such substituents are known for their ability to engage in nucleophilic reactions, enhancing the reactivity profile of the compound. This feature can lead to the development of novel materials in organic synthesis.
  • Application in Solar Cells: Due to its unique electron-donating and accepting properties, compounds like 3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile have gained attention for use in organic solar cells. They can improve energy conversion efficiencies, leading to advancements in renewable energy technologies.
  • Research Potential: Researchers are continually exploring the photophysical behavior of compounds similar to this one in various solvents and environments, contributing to the knowledge of organic electronics. Their findings can open doors to new synthetic routes and applications in optoelectronics.
  • Experimental Techniques: The study of this compound often involves various spectroscopic techniques such as UV-Vis absorption and fluorescence spectroscopy to understand its light-absorbing properties and behavior under different conditions. These techniques contribute extensively to the field of material science.

In conclusion, 3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile is not just a mere chemical compound; it is a potential key player in advancing both organic chemistry and materials science due to its intriguing structure and diverse applications. Continued exploration of its properties could lead to important innovations in technology.

Synonyms
4425-97-2
9,9-Bis(2-cyanoethyl)fluorene
FLUORENE-9,9-DIPROPIONITRILE
9,9-Fluorenedipropionitrile
9H-Fluorene-9,9-dipropanenitrile
9,9'-Fluorenedipropionitrile
Fluorene-9,9-bis(propionitrile)
3-[9-(2-cyanoethyl)fluoren-9-yl]propanenitrile
Propionitrile, 3,3'-fluoren-9-ylidenedi-
NSC-30667
9H-Fluorene-9,9-dipropiononitrile
EINECS 224-605-6
NSC 30667
BRN 2622971
9,9-bis-(2-Cyanoethyl)fluorene
NSC30667
Maybridge1_002232
N7A8T3WAR5
3-09-00-04643 (Beilstein Handbook Reference)
SCHEMBL5866463
HMS547N10
DTXSID10196084
BTB 12648
MFCD00019078
AKOS015840830
Propionitrile,3'-fluoren-9-ylidenedi-
WLN: L B656 HHJ H2CN H2CN
DB-051201
NS00048643
3,3'-(9H-Fluorene-9,9-diyl)dipropanenitrile
BRD-K17782665-001-01-3