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Corannulene

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Identification
Molecular formula
C20H10
CAS number
66444-45-9
IUPAC name
hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene
State
State

Corannulene is a solid at room temperature, showcasing its stability and the robust nature of its aromatic structure.

Melting point (Celsius)
268.00
Melting point (Kelvin)
541.00
Boiling point (Celsius)
530.00
Boiling point (Kelvin)
803.00
General information
Molecular weight
300.37g/mol
Molar mass
300.3690g/mol
Density
1.4810g/cm3
Appearence

Corannulene is a polycyclic aromatic hydrocarbon with a bowl-shaped structure. It appears as a slightly viscous, dark red or reddish-brown crystalline solid when isolated.

Comment on solubility

Solubility Overview of Hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene

Hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene is a complex polycyclic compound. Its solubility characteristics can be summarized as follows:

  • Solvent Dependence: The solubility of this compound largely depends on the solvent used. It is generally more soluble in non-polar solvents due to its hydrophobic nature.
  • Temperature Influence: Increasing temperature may enhance solubility, especially in organic solvents. For example, solubility typically increases with thermal energy.
  • Physical State: In its solid state, it may exhibit limited solubility in water, often requiring organic solvents for effective dissolution.
  • Concentration Effects: As concentration increases, it may reach a saturation point beyond which no additional solute can dissolve.

It is important to note that the complex structure and arrangement of this compound can influence its interaction with solvents, leading to varied solubility profiles across different conditions. In essence, while Hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene is not typically soluble in water, it is essential to explore specific solvent systems and experimental conditions to fully understand its solubility behavior.

Interesting facts

Exploring the Wonders of Hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene

Hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene is an intriguing compound that showcases the intricate nature of carbon chemistry. Here are some fascinating facts about this unique chemical:

  • Complex Structure: This compound features a highly complex bicyclic structure, which is part of what makes it so interesting to chemists. Its connectivity allows for a variety of possible isomeric forms.
  • Potential Applications: Due to its unique structure, hexacyclo compounds like this one may play a role in organic materials, nanotechnology, and even drug design, potentially leading to the development of new therapeutic agents.
  • Natural Occurrence: Similar structures can be found in nature, particularly in certain natural products, indicating that nature often favors complex configurations for functional molecules.
  • Synthesis Challenges: The synthesis of hexacyclic compounds requires advanced synthetic techniques and strategies, including the use of catalysts and protecting groups, highlighting the innovation in chemistry today.
  • Research Significance: Ongoing research into such compounds can reveal insights about stability, reactivity, and electronic properties, which are crucial for the fields of organic chemistry and materials science.

As you delve deeper into the study of chemicals like hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene, remember the words of renowned chemist Linus Pauling: "The best way to have a good idea is to have a lot of ideas." Embrace the complexity and let it inspire your scientific journey!

Synonyms
Benzo[ghi]perylene
191-24-2
1,12-Benzoperylene
1,12-Benzperylene
Benzo[g,h,i]perylene
BENZO(GHI)PERYLENE
Benzo(ghi)pyrilene
Benzo(g,h,i)perylene
Benzo-1,12-perylene
NSC 89275
CCRIS 784
HSDB 6177
UNII-5ZME2E2Q9L
EINECS 205-883-8
benzo(ghi)-perylene
DTXSID5023908
Benzo (g,h,i) perylene
MFCD00004135
NSC-89275
5ZME2E2Q9L
DTXCID303908
hexacyclo[12.8.0.02,11.03,8.04,21.017,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene
CHEBI:34568
BENZO(GHI)PERYLENE [HSDB]
C22H12
Benzo[ghi]perylene; 1,12-Benzoperylene; 1,12-Benzperylene; NSC 89275
1,12Benzperylene
hexacyclo(12.8.0.02,11.03,8.04,21.017,22)docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene
1,12Benzoperylene
1,12-Benoperylene
Benzo[ghi]perylene, 98%
CHEMBL1880376
MSK4307
CS-B0620
NSC89275
Tox21_202732
AKOS015840865
Benzo[ghi]perylene, analytical standard
FB30435
NCGC00163974-01
NCGC00260280-01
CAS-191-24-2
DS-16237
SY051584
DB-044760
B2983
NS00001774
Benzo[ghi]perylene, purum, >=98.0% (GC)
H11449
Benzo[g,h,i]perylene 10 microg/mL in Cyclohexane
Benzo[g,h,i]perylene 10 microg/mL in Acetonitrile
Benzo[g,h,i]perylene 100 microg/mL in Acetonitrile
Q2275328
Benzo[ghi]perylene, vial of 1 g, analytical standard
Benzo[ghi]perylene, BCR(R) certified Reference Material
Benzo[ghi]perylene, certified reference material, TraceCERT(R)
hexacyclo[12.8.0.0(2),(1)(1).0(3),?.0?,(2)(1).0(1)?,(2)(2)]docosa-1(14),2(11),3,5,7,9,12,15,17(22),18,20-undecaene
hexacyclo[12.8.0.0^{2,11.0^{3,8.0^{4,21.0^{17,22]docosa-1(14),2(11),3(8),4,6,9,12,15,17(22),18,20-undecaene