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Coronene

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Identification
Molecular formula
C24H12
CAS number
191-07-1
IUPAC name
hexacyclo[16.3.1.02,7.08,21.011,20.014,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene
State
State

At room temperature, coronene is found in the solid state. It is hydrophobic and a polycyclic aromatic hydrocarbon, making it stable and chemically resistant under standard conditions.

Melting point (Celsius)
438.00
Melting point (Kelvin)
711.15
Boiling point (Celsius)
525.00
Boiling point (Kelvin)
798.15
General information
Molecular weight
300.35g/mol
Molar mass
300.3540g/mol
Density
1.7110g/cm3
Appearence

Coronene typically presents as pale yellow crystals. It is known for its hexagonal structure similar to graphite, giving it a particular aesthetic that is both glossy and crystalline.

Comment on solubility

Solubility of Hexacyclo[16.3.1.02,7.08,21.011,20.014,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene

Hexacyclo[16.3.1.02,7.08,21.011,20.014,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene is a fascinating compound with complex structural characteristics that influence its solubility behavior in various solvents. Here are some key points to consider:

  • Hydrophobicity: Due to its intricate cycloalkane structure, this compound exhibits a significant degree of hydrophobicity, making it less soluble in water.
  • Nonpolar Solvents: It tends to dissolve better in nonpolar solvents such as hexane, toluene, and chloroform, where the solvent-solute interactions can effectively solvate the compound.
  • Temperature Effects: Solubility may improve with increasing temperature, as molecular motion enhances solvation processes, although this will depend on specific conditions.
  • Concentration Considerations: At high concentrations, interactions among solute molecules could lead to decreased solubility due to aggregation, which is common in larger organic compounds.

In summary, the solubility of this compound is predominantly dictated by its highly cyclized structure and its interactions with various solvents. As with many complex organic molecules, understanding these solubility characteristics is crucial for their applications in chemical synthesis and materials science.

Interesting facts

Interesting Facts about Hexacyclo[16.3.1.02,7.08,21.011,20.014,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene

Hexacyclo[16.3.1.02,7.08,21.011,20.014,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene is a fascinating organic compound that belongs to the family of polycyclic hydrocarbons. Its complex cyclic structure is not just chemically intriguing, but it also holds potential implications in various fields of research, particularly in synthetic organic chemistry and material science.

Notable Aspects

  • Complexity of Structure: The compound features multiple interconnected rings, making the study of its chemical properties particularly interesting.
  • Synthetic Utility: Due to its unique molecular architecture, scientists explore its potential applications in creating new materials, pharmaceuticals, and even in electronic devices.
  • Energetics: The stability and reactivity of this compound can provide insights into bonding and interaction in complex organic systems.

This compound is a member of a class known as polycyclic compounds, characterized by multiple interconnected rings. The study of such compounds can help chemists understand fundamental principles such as aromaticity and behavior under various reaction conditions.

Research Implications

Researchers are particularly interested in the following areas:

  • Exploring its potential as a light-harvesting material in solar cells.
  • Investigating possible applications in drug delivery systems due to its unique conformation.
  • Utilizing its properties in the development of advanced polymer materials.

As emphasized by scientists in the field, *"Exploring the complexities of molecular structures opens up new pathways for innovation in materials science."* The journey of understanding Hexacyclo[16.3.1.02,7.08,21.011,20.014,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene is an exciting endeavor that promises to unveil numerous scientific advancements.

Synonyms
Indeno[1,2,3-cd]pyrene
193-39-5
o-Phenylenepyrene
INDENO(1,2,3-CD)PYRENE
1,10-(o-Phenylene)pyrene
1,10-(1,2-Phenylene)pyrene
2,3-Phenylenepyrene
RCRA waste number U137
Indeno[1,2,3-c,d]pyrene
2,3-o-Phenylenepyrene
1,10-(ortho-Phenylene)pyrene
INDENO(1,2,3-C,D)PYRENE
CCRIS 345
HSDB 5101
UNII-T4SWX8I0U2
EINECS 205-893-2
T4SWX8I0U2
BRN 1879312
DTXSID8024153
2,3-(o-Phenylene)pyrene
indeno [1,2,3-cd]pyrene
DTXCID304153
hexacyclo[16.3.1.02,7.08,21.011,20.014,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene
INDENO(1,2,3-CD)PYRENE [HSDB]
INDENO(1,2,3-CD)PYRENE [IARC]
Indeno[1,2,3-c,d]pyrene 10 microg/mL in Cyclohexane
Indeno[1,2,3-c,d]pyrene 10 microg/mL in Acetonitrile
Indeno[1,2,3-c,d]pyrene 100 microg/mL in Acetonitrile
Indeno[1,2,3-c,d]pyrene 100 microg/mL in Cyclohexane
INDENO (1,2,3-cd)PYRENE
INDENO(1,2,3-CD)PYRENE (IARC)
RCRA waste no. U137
oPhenylenepyrene
2,3Phenylenepyrene
hexacyclo(16.3.1.02,7.08,21.011,20.014,19)docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene
Indeno[1,2,3-cd]pyrene; 1,10-(1,2-Phenylene)pyrene; 1,10-(o-Phenylene)pyrene; Indeno[1,2,3-c,d]pyrene; Indeno(1,2,3-c,d)pyrene
2,3oPhenylenepyrene
MFCD00152577
1,10(oPhenylene)pyrene
ORTHO-PHENYLENEPYRENE
1,10(orthoPhenylene)pyrene
1,10(1,2Phenylene)pyrene
indeno (1,2,3-cd) pyrene
Fine dust (PM10-like)-PAHs
CHEMBL3561582
CHEBI:82335
2,3-ORTHO-PHENYLENEPYRENE
Indeno(1,2,3-cd)pyrene solution
Tox21_304020
INDENO(1,2,3-C,D) PYRENE
AKOS015902991
1ST4313
FI30434
NCGC00357288-01
CAS-193-39-5
CS-0102979
NS00008394
Indeno[1,2,3-cd]pyrene, analytical standard
C19251
F82453
Q1838431
Indeno[1,2,3-c,d]pyrene 1000 microg/mL in Acetone
Indeno[1,2,3-cd]pyrene, vial of 1 g, analytical standard
Indeno[1,2,3-cd]pyrene, vial of 25 mg, analytical standard
Indeno[1,2,3-cd]pyrene, certified reference material, TraceCERT(R)
205-893-2
hexacyclo[16.3.1.0^{2,7.0^{8,21.0^{11,20.0^{14,19]docosa-1(22),2,4,6,8(21),9,11(20),12,14(19),15,17-undecaene