Revision as of 14:43, 17 February 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (← Previous edit | Revision as of 18:41, 7 July 2015 edit undoDePiep (talk | contribs)Extended confirmed users294,285 editsm Chembox: rm/replace deprecated params. Fix unknown parameters (via AWB script)Next edit → | ||
Line 2: | Line 2: | ||
| verifiedrevid = 407872079 | | verifiedrevid = 407872079 | ||
| ImageFile = Tetracyclopropylmethane.svg | | ImageFile = Tetracyclopropylmethane.svg | ||
| |
| ImageSize = 150px | ||
| |
| ImageAlt = | ||
| IUPACName = Tetracyclopropylmethane | | IUPACName = Tetracyclopropylmethane | ||
| OtherNames = | | OtherNames = | ||
| |
|Section1={{Chembox Identifiers | ||
| |
| CASNo = 332104-93-5 | ||
| |
| CASNo_Ref = {{cascite|correct|CAS}} | ||
| |
| PubChem = | ||
| |
| SMILES = C1(CC1)C(C2CC2)(C3CC3)C4CC4}} | ||
| |
|Section2={{Chembox Properties | ||
| |
| C=13 | H=20 | ||
| |
| Appearance = | ||
| |
| Density = | ||
| |
| MeltingPt = | ||
| |
| BoilingPt = | ||
| |
| Solubility = }} | ||
| |
|Section3={{Chembox Hazards | ||
| |
| MainHazards = | ||
| |
| FlashPt = | ||
| |
| AutoignitionPt = }} | ||
}} | }} | ||
Revision as of 18:41, 7 July 2015
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.
{{cite journal}}
: CS1 maint: multiple names: authors list (link)
This article about a hydrocarbon is a stub. You can help Misplaced Pages by expanding it. |