Interesting facts
              Interesting Facts About 8-Iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene
8-Iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene is a fascinating compound that belongs to the family of polycyclic aromatic hydrocarbons. Here are some interesting aspects that highlight its significance in the field of organic chemistry:
- Structural Complexity: This compound features a unique and intricate structure consisting of multiple interlocking rings, making it a valuable subject for studying ring strain and molecular stability.
- Role of Iodine: The presence of iodine not only influences the reactivity of the compound but also imparts interesting electronic properties. Iodine can play a crucial role in various reactions, including electrophilic substitutions.
- Polycyclic Aromatic Hydrocarbons: As a member of this family, it shares characteristics with other well-known compounds like naphthalene and anthracene, which have applications in materials science and organic electronics.
- Potential Applications: Due to its unique properties, this compound could have potential applications in organic synthesis and might serve as an intermediate in the development of pharmaceuticals and advanced materials.
- Importance in Research: Compounds with intricate structures such as this one can help chemists understand fundamental concepts of molecular interactions, stability, and reactivity. As a result, they are often the focus of advanced research in synthetic organic chemistry.
As with many complex organic compounds, the study of 8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene opens doors to a deeper understanding of chemical structures and reactivity, leading to potential innovations in various fields.
Synonyms
          Diphenyleneiodonium
          Dibenziodolium
          244-54-2
          Diphenylene iodonium
          2,2'-Biphenylyleneiodonium
          dibenzo[b,d]iodolium
          (1,1'-Biphenyl)-2,2'-diyliodonium
          Dibenzo[b,d]iodol-5-ium
          diphenyl-iodonium hydrochloride
          CHEBI:77986
          6HJ411TU98
          8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene
          CHEMBL397686
          UNII-6HJ411TU98
          Tocris-0504
          1010-76-0
          Lopac-D-2926
          Lopac0_000367
          BSPBio_001027
          KBioGR_000367
          KBioSS_000367
          SCHEMBL219548
          CHEMBL365739
          KBio2_000367
          KBio2_002935
          KBio2_005503
          KBio3_000713
          KBio3_000714
          QFXKXRXFBRLLPQ-UHFFFAOYSA-
          DTXSID00924595
          Bio1_000428
          Bio1_000917
          Bio1_001406
          Bio2_000344
          Bio2_000824
          HMS1362C09
          HMS1792C09
          HMS1990C09
          HMS3403C09
          BDBM50206334
          CCG-204462
          IDI1_002099
          QTL1_000031
          NCGC00015334-01
          NCGC00015334-02
          NCGC00015334-03
          NCGC00015334-04
          NCGC00015334-05
          NCGC00015334-06
          NCGC00015334-07
          NCGC00015334-09
          NCGC00015334-13
          NCGC00024620-01
          NCGC00024620-02
          NCGC00024620-03
          NCGC00024620-04
          NS00015673
          BRD-K65814004-001-02-3
          BRD-K65814004-003-01-1
          BRD-K65814004-003-02-9
          Q27147567
          InChI=1/C12H8I/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H/q+1
              
Solubility of 8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene (C13H9I)
The solubility of 8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene, characterized by its unique structural arrangement, is an intriguing topic in the field of chemical science. This compound, containing an iodine atom, presents interesting interactions with solvents. Here are some key points regarding its solubility:
In summary, the solubility characteristics of C13H9I are influenced by its molecular structure, the inherent properties of iodine, and the nature of interactions with various solvents. As with many organic halides, it demonstrates a preference for nonpolar environments.