| Revision as of 23:38, 18 February 2016 editHeadbomb (talk | contribs)Edit filter managers, Autopatrolled, Extended confirmed users, Page movers, File movers, New page reviewers, Pending changes reviewers, Rollbackers, Template editors454,513 editsm →top: standardize Angew Chem., replaced: Angewandte Chemie, International Edition → Angewandte Chemie International Edition, added orphan tag using AWB← Previous edit | Revision as of 03:22, 6 June 2016 edit undoDcirovic (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers253,275 editsm →top: refs using AWBNext edit → | ||
| Line 28: | Line 28: | ||
| '''Tetracyclopropylmethane''' is an ], a ] ] with formula C<sub>13</sub>H<sub>20</sub>, or (C<sub>3</sub>H<sub>5</sub>-)<sub>4</sub>C. The ] skeleton of its molecule consists of four ] rings attached to a central carbon atom. | '''Tetracyclopropylmethane''' is an ], a ] ] with formula C<sub>13</sub>H<sub>20</sub>, or (C<sub>3</sub>H<sub>5</sub>-)<sub>4</sub>C. The ] skeleton of its molecule consists of four ] rings attached to a central carbon atom. | ||
| This compound was synthesized in 2001 by ] and others, with ] as an intermediate step.<ref>{{cite journal | doi = 10.1002/1521-3773(20010105)40:1<180::AID-ANIE180>3.0.CO;2-K | |
This compound was synthesized in 2001 by ] and others, with ] as an intermediate step.<ref>{{cite journal | doi = 10.1002/1521-3773(20010105)40:1<180::AID-ANIE180>3.0.CO;2-K |author1=Kozhushkov, Sergei I. |author2=Kostikov, Rafael R. |author3=Molchanov, Alexander P. |author4=Boese, Roland |author5=Benet-Buchholz, Jordi |author6=Schreiner, Peter R. |author7=Rinderspacher, Christopher |author8=Ghiviriga, Ion |author9=De Meijere, Armin. | title = Tetracyclopropylmethane: a unique hydrocarbon with S4 symmetry | journal = Angewandte Chemie International Edition | year = 2001 | volume = 40 | issue = 1 | pages = 180–183}}</ref> In the solid state, the molecules have a propeller shape with S4 symmetry. | ||
| ==References== | ==References== | ||
Revision as of 03:22, 6 June 2016
 | This article is an orphan, as no other articles link to it. Please introduce links to this page from related articles; try the Find link tool for suggestions. (February 2016) |
| |
| Names | |
|---|---|
| IUPAC name Tetracyclopropylmethane | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| CompTox Dashboard (EPA) | |
SMILES
| |
| Properties | |
| Chemical formula | C13H20 |
| Molar mass | 176.303 g·mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
 Y verify (what is ?)
Infobox references
| |
Tetracyclopropylmethane is an organic compound, a polycyclic hydrocarbon with formula C13H20, or (C3H5-)4C. The carbon skeleton of its molecule consists of four cyclopropane rings attached to a central carbon atom.
This compound was synthesized in 2001 by Armin de Meijere and others, with dicyclopropyldiethenylmethane as an intermediate step. In the solid state, the molecules have a propeller shape with S4 symmetry.
References
- Kozhushkov, Sergei I.; Kostikov, Rafael R.; Molchanov, Alexander P.; Boese, Roland; Benet-Buchholz, Jordi; Schreiner, Peter R.; Rinderspacher, Christopher; Ghiviriga, Ion; De Meijere, Armin. (2001). "Tetracyclopropylmethane: a unique hydrocarbon with S4 symmetry". Angewandte Chemie International Edition. 40 (1): 180–183. doi:10.1002/1521-3773(20010105)40:1<180::AID-ANIE180>3.0.CO;2-K.
 | This article about a hydrocarbon is a stub. You can help Misplaced Pages by expanding it. |