| 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 |
Latest revision as of 11:45, 21 October 2024 edit undoJWBE (talk | contribs)Extended confirmed users10,111 edits removed Category:Cyclopropanes; added Category:Cyclopropyl compounds using HotCat |
| (10 intermediate revisions by 8 users not shown) |
| Line 1: |
Line 1: |
|
{{Chembox |
|
{{Chembox |
|
|
| Verifiedfields = changed |
|
| verifiedrevid = 407872079 |
|
| verifiedrevid = 414439250 |
|
| ImageFile = Tetracyclopropylmethane.svg |
|
| ImageFile = Tetracyclopropylmethane.svg |
|
| ImageSize = 150px |
|
| ImageSize = 150px |
|
| ImageAlt = |
|
| ImageAlt = |
|
|
| PIN = 1,1′,1′′,1′′′-Methanetetrayltetracyclopropane |
|
| IUPACName = Tetracyclopropylmethane |
|
|
| OtherNames = |
|
| OtherNames = |
|
| Section1 = {{Chembox Identifiers |
|
|Section1={{Chembox Identifiers |
|
| CASNo = 332104-93-5 |
|
| CASNo = 332104-93-5 |
|
| CASNo_Ref = {{cascite|correct|CAS}} |
|
| CASNo_Ref = {{cascite|correct|CAS}} |
|
| PubChem = |
|
| PubChem = 57417320 |
|
|
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
| ⚫ |
| SMILES = C1(CC1)C(C2CC2)(C3CC3)C4CC4}} |
|
|
|
| ChemSpiderID = 35765346 |
| ⚫ |
| Section2 = {{Chembox Properties |
|
|
⚫ |
| SMILES = C1(CC1)C(C2CC2)(C3CC3)C4CC4 |
| ⚫ |
| C=13 | H=20 |
|
|
|
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
|
| Appearance = |
|
|
|
| StdInChI = 1S/C13H20/c1-2-9(1)13(10-3-4-10,11-5-6-11)12-7-8-12/h9-12H,1-8H2 |
|
| Density = |
|
|
|
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
|
| MeltingPt = |
|
|
|
| StdInChIKey = KXAOPBGXMXVCRN-UHFFFAOYSA-N}} |
| ⚫ |
| BoilingPt = |
|
|
⚫ |
|Section2={{Chembox Properties |
| ⚫ |
| Solubility = }} |
|
|
⚫ |
| C=13 | H=20 |
| ⚫ |
| Section3 = {{Chembox Hazards |
|
|
| MainHazards = |
|
| Appearance = |
|
| FlashPt = |
|
| Density = |
|
| Autoignition = }} |
|
| MeltingPt = |
|
⚫ |
| BoilingPt = |
|
⚫ |
| Solubility = }} |
|
⚫ |
|Section3={{Chembox Hazards |
|
|
| MainHazards = |
|
|
| FlashPt = |
|
|
| AutoignitionPt = }} |
|
}} |
|
}} |
|
|
|
|
|
'''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 | author = Kozhushkov, Sergei I.; Kostikov, Rafael R.; Molchanov, Alexander P.; Boese, Roland; Benet-Buchholz, Jordi; Schreiner, Peter R.; Rinderspacher, Christopher; Ghiviriga, Ion; 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. |
|
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== |
|
{{Reflist}} |
|
{{Reflist}} |
|
|
|
|
|
] |
|
] |
|
|
|
|
|
|
|
|