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2-chlorophenanthrene

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Identification
Molecular formula
C14H9Cl
CAS number
19009-56-4
IUPAC name
2-chlorophenanthrene
State
State
2-Chlorophenanthrene is a solid at room temperature. The compound remains in this state under standard conditions, due to its polycyclic aromatic structure.
Melting point (Celsius)
99.00
Melting point (Kelvin)
372.15
Boiling point (Celsius)
372.00
Boiling point (Kelvin)
645.15
General information
Molecular weight
230.68g/mol
Molar mass
230.6960g/mol
Density
1.2560g/cm3
Appearence

2-Chlorophenanthrene is known to appear as a white to pale yellow crystalline solid. The compound's appearance is typical for polyaromatic hydrocarbons, characterized by its distinct arrangement of fused aromatic rings, contributing to its solid nature.

Comment on solubility

Solubility of 2-chlorophenanthrene

2-chlorophenanthrene, a derivative of phenanthrene, exhibits intriguing solubility characteristics that are essential for various chemical applications. Its solubility can be influenced by several factors:

  • Polarity: Due to the presence of the chloro group, 2-chlorophenanthrene has increased polarity compared to its parent compound, phenanthrene. This impact can enhance its solubility in polar solvents.
  • Temperature: Like many organic compounds, the solubility of 2-chlorophenanthrene tends to increase with temperature, making it more soluble in hot solvents.
  • Solvent Type: It is typically more soluble in organic solvents, such as ethyl acetate or benzene, and less soluble in water. This behavior is attributed to hydrophobic interactions that favor solvation in non-polar environments.

To summarize, the solubility of 2-chlorophenanthrene is largely influenced by its molecular structure and the nature of the solvent used. Understanding these parameters is vital for effective use in chemical processes, highlighting the importance of selecting the appropriate medium for dissolution.

Interesting facts

Interesting Facts about 2-Chlorophenanthrene

2-Chlorophenanthrene is a fascinating organic compound that belongs to the class of chlorinated polycyclic aromatic hydrocarbons (PAHs). It is derived from phenanthrene, which means it consists of three fused benzene rings with a chlorine atom substituted in the second position. This unique structure contributes to its properties and potential applications.

Key Aspects of 2-Chlorophenanthrene

  • Environmental Impact: As a chlorinated compound, 2-chlorophenanthrene has garnered attention due to its persistence in the environment and potential for bioaccumulation. Studying its environmental behavior helps scientists understand the broader implications of PAHs.
  • Health Considerations: Compounds like 2-chlorophenanthrene are often scrutinized due to their possible carcinogenicity. Understanding how chlorinated PAHs interact with biological systems is critical for public health.
  • Industrial Relevance: This compound can be utilized in various chemical reactions, particularly in synthetic organic chemistry. Researchers explore its properties to develop new materials or chemical processes.
  • Research Applications: 2-Chlorophenanthrene is often used in laboratories for studying the effects of chlorinated compounds on living organisms and ecosystems, making it an important subject in environmental sciences.

In summary, 2-chlorophenanthrene serves as a striking example of how the structure of a compound can influence its behavior in both environmental and biological contexts. With its complex properties and diverse applications, it provides a rich area for further exploration and understanding in the field of chemistry.

Synonyms
2-CHLOROPHENANTHRENE
24423-11-8
DTXSID10179175
RefChem:259538
DTXCID40101666
MFCD13191757
phenanthrene, 2-chloro-
SCHEMBL1392239
SCHEMBL2723778
SCHEMBL6436724
CHEMBL1797286
MSK179748
AKOS015851312
BS-16282
SY278310
DB-022396
CS-0155966
D82506
423C118
F232377