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5-Methylbenzo[c]phenanthrene

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Identification
Molecular formula
C19H14
CAS number
192-69-0
IUPAC name
5-methylbenzo[c]phenanthrene
State
State

At room temperature, 5-methylbenzo[c]phenanthrene is typically in a solid state due to the high melting point of polycyclic aromatic hydrocarbons.

Melting point (Celsius)
114.00
Melting point (Kelvin)
387.15
Boiling point (Celsius)
481.20
Boiling point (Kelvin)
754.40
General information
Molecular weight
254.33g/mol
Molar mass
254.3270g/mol
Density
1.2091g/cm3
Appearence

5-Methylbenzo[c]phenanthrene typically appears as a pale yellow or white crystalline solid. The compound is often found in a crystalline form due to its polycyclic aromatic structure.

Comment on solubility

Solubility of 5-methylbenzo[c]phenanthrene

5-methylbenzophenanthrene, a polycyclic aromatic hydrocarbon, exhibits particular solubility characteristics that are crucial for understanding its behavior in various environments.

Here are some key points regarding its solubility:

  • Hydrophobic Nature: As a large, complex aromatic compound, 5-methylbenzophenanthrene tends to be hydrophobic, making it poorly soluble in water.
  • Solvent Compatibility: It is generally more soluble in organic solvents like:
    • Hexane
    • Toluene
    • Xylene
  • Temperature Effects: Solubility may increase with temperature, particularly in organic solvents, as higher temperatures can enhance the interactions between solute and solvent molecules.

In summary, the solubility behavior of 5-methylbenzophenanthrene is primarily dictated by its hydrophobicity and compatibility with organic solvents, making it an important compound to consider in contexts such as environmental science and chemical applications.

Interesting facts

Interesting Facts about 5-Methylbenzo[c]phenanthrene

5-Methylbenzophenanthrene is a fascinating polycyclic aromatic hydrocarbon (PAH) that attracts attention due to its unique structural and chemical characteristics. Here are some engaging insights:

  • Structure and Isomerism: This compound features a complex arrangement of carbon rings, making it a member of the benzanthracene family. Its structure allows for various isomeric forms, showcasing the versatility found in organic compounds.
  • Environmental Relevance: 5-Methylbenzophenanthrene is found in environmental samples and is a byproduct of incomplete combustion processes. As a result, it is often studied for its potential impact on air and soil quality.
  • Toxicity Potential: Like many PAHs, this compound has been researched for its carcinogenic properties. Understanding the implications of exposure to such compounds is crucial for both public health and environmental safety.
  • Research Significance: The study of 5-methylbenzophenanthrene contributes to the larger field of organic chemistry, particularly in understanding how complex hydrocarbons behave, their synthesis, and their reactivity with other chemicals.
  • Applications in Material Science: Due to its unique electronic properties, compounds like 5-methylbenzophenanthrene are also being explored for applications in organic electronics, such as organic semiconductors and photovoltaic devices.

In conclusion, 5-methylbenzophenanthrene provides a wealth of information for chemists and researchers alike. Its study not only enhances our understanding of complex organic molecules but also informs our knowledge about environmental impact and material applications.

Synonyms
5-Methylbenzo[c]phenanthrene
5-Methylbenzo(c)phenanthrene
5-Methyl-3,4-benzophenanthrene
Benzo[c]phenanthrene, 5-methyl-
BENZO(c)PHENANTHRENE, 5-METHYL-
NSC 135889
BRN 2329427
DTXSID70215503
4-05-00-02571 (Beilstein Handbook Reference)
DTXCID30137994
620-753-4
pseuamgcksrkql-uhfffaoysa-n
652-04-0
2-Methyl-3,4-benzphenanthrene
NSC-135889
NSC135889
Y5UBE249AB
2-Methyl-3,4-benzphenanthren
WLN: L C6 B666J I1
AKOS024340894