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9-Chlorophenanthrene

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Identification
Molecular formula
C14H9Cl
CAS number
2521-92-6
IUPAC name
9-chlorophenanthrene
State
State

At room temperature, 9-Chlorophenanthrene is a solid. It is crystalline and typically appears in a yellow color.

Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
468.50
Boiling point (Kelvin)
741.70
General information
Molecular weight
216.68g/mol
Molar mass
216.6750g/mol
Density
1.2740g/cm3
Appearence

9-Chlorophenanthrene appears as a yellow crystalline solid. It is often used in chemical research and can be seen exhibiting a crystalline form with a distinct yellowish color.

Comment on solubility

Solubility of 9-Chlorophenanthrene

9-Chlorophenanthrene, with the chemical formula C14H9Cl, exhibits unique solubility characteristics that are important to understand. This aromatic compound is generally considered to have low solubility in water, making it a hydrophobic substance. The solubility profile can be summarized as follows:

  • Water Solubility: 9-Chlorophenanthrene is insoluble in water. Its nonpolar nature contributes to this lack of solubility, as water is a polar solvent.
  • Organic Solvents: This compound is typically soluble in nonpolar organic solvents such as:
    • Benzene
    • Toluene
    • Chloroform
  • Temperature Effect: Solubility in organic solvents can increase with temperature, enabling better dissolution in practical applications.

Overall, due to its hydrophobic nature and preference for organic environments, 9-chlorophenanthrene displays a distinctive pattern of solubility that is critical for its utility in various chemical processes.

Interesting facts

Interesting Facts about 9-Chlorophenanthrene

9-Chlorophenanthrene is a fascinating compound for several reasons, ranging from its structure to its applications in various fields. Here are some notable points:

  • Unique Structure: The compound features a chlorinated phenanthrene skeleton, which is significant in the study of polycyclic aromatic hydrocarbons (PAHs). Its unique configuration allows it to interact with biological systems in intriguing ways.
  • Environmental Relevance: As a chlorinated compound, it raises concerns regarding environmental toxicity and persistence. Researchers are particularly interested in its potential as a pollutant, as it can serve as a model for understanding the behavior of similar compounds in ecosystems.
  • Biological Activity: Studies have shown that 9-chlorophenanthrene can exhibit biological activity that may influence cellular responses. This makes it a compound of interest in pharmacological research and toxicology.
  • Research Applications: In the field of materials science, compounds like 9-chlorophenanthrene are explored for potential use in developing organic electronic devices, including organic light-emitting diodes (OLEDs) and organic solar cells.
  • Synthesis: The synthesis of 9-chlorophenanthrene offers chemists avenues to explore various reaction mechanisms and pathways, enhancing the understanding of chemical transformations in organic chemistry.

In conclusion, 9-chlorophenanthrene is more than just a chemical entity; it represents the intersection of environmental science, chemistry, and materials research. As scientists continue to study its properties and applications, this compound remains a topic of ongoing inquiry and exploration.

Synonyms
9-CHLOROPHENANTHRENE
947-72-8
Phenanthrene, 9-chloro-
CCRIS 5543
NSC 8552
EINECS 213-430-0
BRN 2047058
AI3-24095
DTXSID00241572
DTXCID30164063
213-430-0
4-05-00-02303 (beilstein handbook reference)
cjwhzqnudajjsb-uhfffaoysa-n
10-Chlorophenanthrene
NSC8552
Phenanthrene, 9-chloro-; 9-Chlorophenanthrene; 10-Chlorophenanthrene; NSC 8552
SCHEMBL1922076
CHEMBL1986631
NSC-8552
MFCD00037142
AKOS015851129
BS-33293
SY297986
DB-057530
CS-0207071
NS00040418
G82929