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1-nitrofluoranthene

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Identification
Molecular formula
C16H9NO2
CAS number
13349-61-6
IUPAC name
1-nitrofluoranthene
State
State

At room temperature, 1-nitrofluoranthene exists as a solid.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
426.00
Boiling point (Kelvin)
699.15
General information
Molecular weight
247.25g/mol
Molar mass
247.2430g/mol
Density
1.4327g/cm3
Appearence

1-Nitrofluoranthene is typically a solid compound at room temperature. It generally appears as a yellow crystalline powder and can have a distinct odor. It is known for its bright yellow color typical of many nitroaromatic compounds.

Comment on solubility

Solubility of 1-nitrofluoranthene

1-nitrofluoranthene, with the chemical formula C13H9NO2, exhibits distinct solubility characteristics that are important for various applications. Understanding its solubility can help predict its behavior in different environments. Here are some key points:

  • Polarity: 1-nitrofluoranthene is a polar compound due to the presence of the nitro group (-NO2), which affects its solubility in solvents.
  • Solvent Compatibility: It tends to be more soluble in polar organic solvents such as acetone, ethanol, and methanol.
  • Water Solubility: Given its structure, 1-nitrofluoranthene has a low solubility in water, making it challenging to dissolve in aqueous solutions.
  • Environmental Implications: Its solubility profile impacts its mobility and bioavailability in environmental contexts, especially in soil and aquatic systems.

In summary, the solubility of 1-nitrofluoranthene is significantly influenced by its polarity and the nature of the solvent, paving the way for various applications and implications in environmental science. As one might say, "Solubility is the key to unlocking a compound's potential!"

Interesting facts

Interesting Facts About 1-Nitrofluoranthene

1-Nitrofluoranthene is a fascinating organic compound belonging to the family of polycyclic aromatic hydrocarbons (PAHs) and is known for its distinctive properties and potential applications. Here are some enlightening facts about this compound:

  • Structure and Reactivity: The presence of a nitro group (-NO2) on the fluoranthene skeleton enhances its reactivity, making 1-nitrofluoranthene a subject of interest for various chemical reactions, including electrophilic aromatic substitution.
  • Environmental Impacts: Like many PAHs, 1-nitrofluoranthene can be found in environmental pollutants, particularly from incomplete combustion of organic matter. Its environmental behavior is crucial for understanding pollution and remediation processes.
  • Biological Effects: Studies have suggested that nitro-PAHs, including 1-nitrofluoranthene, could exhibit mutagenic and carcinogenic properties, making them important targets for toxicology research.
  • Analytical Importance: 1-Nitrofluoranthene is often analyzed in environmental samples to monitor PAH contamination levels, serving as a marker of environmental health and pollution control.

Researchers and students alike find 1-nitrofluoranthene particularly intriguing due to its dual role in environmental science and synthetic chemistry. As we continue to explore the complexities of such compounds, we uncover new avenues for application and deeper understanding of their implications.

As Albert Einstein once said, “The important thing is not to stop questioning. Curiosity has its own reason for existence.” This sentiment rings true for the ongoing study of compounds like 1-nitrofluoranthene, where each investigation unravels new mysteries of the chemical world.


Synonyms
1-Nitrofluoranthene
Fluoranthene, 1-nitro-
CCRIS 5509
BRN 2562309
87UV3TW2B9
DTXSID00157200
4-05-00-02465 (Beilstein Handbook Reference)
DTXCID4079691
awyzhupawkzjsl-uhfffaoysa-n
13177-28-1
1-Nitro-fluoranthene
NITROFLUORANTHENE
UNII-87UV3TW2B9
CHEMBL351184
SCHEMBL4377088
DB-216190