Difference between revisions of "Methylenecyclohexane"
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'''Methylenecyclohexane''' is a very useful compound in [[organic syntheses]]. It can be produced by a [[Wittig reaction]] or a [[Tebbe reaction]] from [[cyclohexanone]], or as a side product of the dehydration of 2-methylcyclohexanol into methylcyclohexene. | '''Methylenecyclohexane''' is a very useful compound in [[organic syntheses]]. It can be produced by a [[Wittig reaction]] or a [[Tebbe reaction]] from [[cyclohexanone]], or as a side product of the dehydration of 2-methylcyclohexanol into methylcyclohexene. | ||
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[[Category:Alkenes]] | [[Category:Alkenes]] | ||
{{Imported from Wikipedia|name=Methylenecyclohexane|id=308469232}} | {{Imported from Wikipedia|name=Methylenecyclohexane|id=308469232}} | ||
Latest revision as of 19:36, 22 August 2009
| Methylenecyclohexane | |
|---|---|
| |
| IUPAC name | methylenecyclohexane |
| Identifiers | |
| InChI | InChI=1/C7H12/c1-7-5-3-2-4-6-7/h1-6H2 |
| InChIKey | YULMNMJFAZWLLN-UHFFFAOYAJ |
| Standard InChI | InChI=1S/C7H12/c1-7-5-3-2-4-6-7/h1-6H2 |
| Standard InChIKey | YULMNMJFAZWLLN-UHFFFAOYSA-N |
| CAS number | [] |
| EC number | |
| ChemSpider | |
| PubChem | |
| SMILES | |
| Properties | |
| Chemical formula | C7H12 |
| Molar mass | 96.170 g/mol |
| Hazards | |
| EU index number | not listed |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Methylenecyclohexane is a very useful compound in organic syntheses. It can be produced by a Wittig reaction or a Tebbe reaction from cyclohexanone, or as a side product of the dehydration of 2-methylcyclohexanol into methylcyclohexene.
References
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This page was originally imported from Wikipedia, specifically this version of the article "Methylenecyclohexane". Please see the history page on Wikipedia for the original authors. This WikiChem article may have been modified since it was imported. It is licensed under the Creative Commons Attribution–Share Alike 3.0 Unported license. |
