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7H-Benzo[c]fluoren-7-one

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Identification
Molecular formula
C17H10O
CAS number
3074-00-8
IUPAC name
benzo[c]fluoren-7-one
State
State

The compound is in a solid state at room temperature. It is not volatile and typically requires solvent to be mobilized for chemical reactions.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.20
Boiling point (Celsius)
460.60
Boiling point (Kelvin)
733.80
General information
Molecular weight
230.27g/mol
Molar mass
230.2530g/mol
Density
1.2560g/cm3
Appearence

7H-Benzo[c]fluoren-7-one typically appears as a yellow crystalline solid. It is known for its bright color and is used in research due to its chromophoric properties.

Comment on solubility

Solubility of Benzo[c]fluoren-7-one

Benzo[c]fluoren-7-one, with the chemical formula C14H10O, exhibits limited solubility characteristics that are important to understand for its applications in various chemical contexts.

Key points regarding its solubility include:

  • Solvent Behavior: Benzo[c]fluoren-7-one is primarily soluble in organic solvents such as ether, benzene, and chloroform. This behavior is typical for polycyclic aromatic ketones, which tend to dissolve well in non-polar solutions.
  • Aqueous Solubility: It has very low solubility in water, which is not uncommon due to its hydrophobic character. When considering reactions or extractions, this property can be advantageous.
  • Impact of Temperature: Solubility can vary significantly with temperature; often, organic compounds experience increased solubility at elevated temperatures.

Overall, understanding the solubility profile of benzo[c]fluoren-7-one is crucial for effective use in synthesis and research, ensuring maximized efficacy in organic reactions. As stated, "like dissolves like," and hence, the use of compatible solvents is key to realizing its full potential.

Interesting facts

Interesting Facts about Benzo[c]fluoren-7-one

Benzo[c]fluoren-7-one is a fascinating organic compound that belongs to the class of polycyclic aromatic hydrocarbons (PAHs). Here are some engaging aspects of this intriguing molecule:

  • Structural Uniqueness: Benzo[c]fluoren-7-one features a distinctive fused ring system, which contributes to its stability and aromatic character. The structure includes a ketone functional group that adds to its chemical reactivity.
  • Applications in Research: This compound is utilized in various fields of research, particularly in the areas of organic electronics and photonics. Its ability to serve as an electron transport material makes it significant in the development of organic light-emitting diodes (OLEDs).
  • Fluorescence Properties: Benzo[c]fluoren-7-one is known for its notable optical properties. It exhibits fluorescence under certain conditions, which is advantageous for applications in fluorescence microscopy and sensor technologies.
  • Natural Occurrence: Interestingly, compounds related to benzo[c]fluoren-7-one can be found in certain natural sources, including some plant materials, where they contribute to the complex chemistry of their secondary metabolites.
  • Environmental Concerns: As a member of the PAHs, benzo[c]fluoren-7-one also raises environmental concerns due to its potential carcinogenic effects. Understanding its behavior in the environment is crucial for assessing risks related to pollution.

In conclusion, benzo[c]fluoren-7-one is not only a compound of structural elegance but also one of practical importance, crossing the boundaries of chemistry, technology, and environmental science. Its varied applications and intriguing properties continue to inspire research and innovation in modern chemistry.

Synonyms
7H-benzo[c]fluoren-7-one
6051-98-5
Allochrysoketone
7H-BENZO(C)FLUOREN-7-ONE
CCRIS 3168
DTXSID00209258
DTXCID20131749
usywcedyvlpnhh-uhfffaoysa-n
benzo[c]fluoren-7-one
allo-Chrysoketone
7H-Benzo[c]fluorene-7-one
MFCD00215961
SCHEMBL3922177
DB-359854
Allochrysoketone; 7H-Benz[c]fluoren-7-one;
B6180
E78980