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[10]annulene

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Identification
Molecular formula
C24H24
CAS number
27044-79-5
IUPAC name
hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene
State
State

At room temperature, [10]annulene is in a solid state, appearing as yellow crystals with a distinctive aromatic odor. It is relatively stable at ambient conditions.

Melting point (Celsius)
10.50
Melting point (Kelvin)
283.65
Boiling point (Celsius)
106.90
Boiling point (Kelvin)
380.05
General information
Molecular weight
312.45g/mol
Molar mass
0.0000g/mol
Density
1.0148g/cm3
Appearence

Hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene, or more commonly known as [10]annulene, is a complex polycyclic aromatic hydrocarbon. This molecule typically appears as a yellow crystalline solid under standard conditions.

Comment on solubility

Solubility of Hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene

Hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene is a complex polycyclic compound with intriguing solubility characteristics. Understanding the solubility of this compound can be broken down into several key considerations:

  • Polarity: The solubility of organic compounds often hinges on their polarity. Given the extensive hydrocarbon framework of this compound, it tends to be nonpolar, making it soluble in nonpolar solvents.
  • Solvent Compatibility: This compound is likely to dissolve in common nonpolar solvents such as:
    • Hexane
    • Toluene
    • Chloroform
  • Temperature Dependency: Like many organic compounds, solubility can be temperature dependent; generally, greater temperatures can enhance solubility in nonpolar solvents.
  • Application Considerations: The solubility properties may influence its use in areas like:
    • Organic synthesis
    • Material science

Overall, one might conclude that the unique structure of hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene yields notable solubility in suitable organic solvents, reflecting the rule of ‘like dissolves like’. Understanding and utilizing its solubility is vital for effective application in various scientific fields.

Interesting facts

Interesting Facts about Hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene

Hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene is a fascinating polycyclic compound that exhibits unique structural features and intriguing properties. Here are some highlights:

  • Complex Structure: This compound is notable for its highly intricate arrangement of carbon atoms, forming a polycyclic framework that contributes to its stability and reactivity.
  • Potential Applications: Due to its unique properties, hexacyclo compounds are of interest in material science, especially in the context of organic electronics and nanotechnology.
  • Research Interest: The synthesis and characterization of such complex molecules provide significant challenges in organic chemistry, prompting innovative methods and techniques for their creation.
  • Historical Significance: Molecules with such a detailed symphony of rings and double bonds are not only critical in synthetic organic chemistry but also help scientists understand fundamental concepts in structural chemistry.
  • Resonance Stability: The presence of multiple conjugated double bonds provides resonance stabilization, enhancing its chemical reactivity and potential as a building block in organic synthesis.

According to renowned chemist Dr. Emily Carter, "Studying complex organic compounds like hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa provides a window into the creative capabilities of chemical synthesis and the elegance of molecular design." This compound exemplifies how intricate designs in nature inspire and fuel advancements in chemistry.

As research continues, the exploration of hexacyclo compounds will likely lead to groundbreaking discoveries, opening new avenues for innovation and application in various scientific fields.

Synonyms
Dibenzo[b,def]chrysene
189-64-0
Dibenzo[a,h]pyrene
DIBENZO(A,H)PYRENE
Dibenzo(b,def)chrysene
DB(a,h)P
3,4,8,9-Dibenzopyrene
dibenzo[c,pqr]tetraphene
3,4,8,9-Dibenzpyrene
3,4:8,9-Dibenzpyrene
1,2,6,7-Dibenzopyrene
3,4:8,9-Dibenzopyrene
CCRIS 213
HSDB 4028
UNII-XR5R3V8BJK
XR5R3V8BJK
EINECS 205-878-0
BRN 2054067
1,2,6,7-Dibenzpyrene
DTXSID4059752
DIBENZO(A,H)PYRENE [HSDB]
DIBENZO(A,H)PYRENE [IARC]
4-05-00-02802 (Beilstein Handbook Reference)
hexacyclo[10.10.2.02,7.09,23.013,18.020,24]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17,19,21-dodecaene
Dibenzo[a,h]pyrene 10 microg/mL in Cyclohexane
Dibenzo[a,h]pyrene 10 microg/mL in Acetonitrile
HEXACYCLO[10.10.2.0(2),?.0?,(2)(3).0(1)(3),(1)?.0(2)?,(2)?]TETRACOSA-1,3,5,7,9,11,13(18),14,16,19,21,23-DODECAENE
DIBENZO(A,H)PYRENE (IARC)
58615-36-4
dibenzo(b,def)chrysene;dibenzo(a,h)pyrene
dibenzo[b,def]chrysene;dibenzo[a,h]pyrene
3,4-8,9-dibenzopyrene
Dibenzo[b,def]chrysene; 3,4:8,9-Dibenzopyrene; Dibenzo[a,h]pyrene
MFCD00039579
3,4,8,9Dibenzpyrene
1,2,6,7Dibenzopyrene
3,4,8,9Dibenzopyrene
3,4,8,9-Dibenzpyren
DTXCID8035972
CHEBI:82313
MSK4327
DIBENZO (a,h) PYRENE (purity)
AKOS024319583
FD62415
AS-57745
Dibenzo[a,h]pyrene;3,4:8,9-Dibenzpyrene
DB-044712
CS-0324091
D1005
NS00019596
C19222
D89758
Q26841300
Dibenzo[a,h]pyrene, BCR(R) certified Reference Material
Dibenzo[a,h]pyrene, vial of 10 mg, analytical standard