1-Bromoadamantane
1-Bromoadamantane is the organobromine compound with the formula (CH2)6(CH)3CBr. A colorless solid, the compound is a derivative of adamantane with a bromine atom at one of the four equivalent methine positions. Classified as a tertiary alkyl bromide, it is reluctant to form organometallic derivatives. With Rieke calcium however it forms the organocalcium derivative, which functions like a Grignard reagent.[1]
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| Names | |
|---|---|
| Preferred IUPAC name 1-Bromoadamantane | |
| Other names 1-Adamantyl bromide, adamantane, 1-bromo-, adamantyl bromide, tricyclo[3.3.1.1(3,7)]decane, 1-bromo- | |
| Identifiers | |
| 3D model (JSmol) | |
| 1098857 | |
| ChemSpider | |
| ECHA InfoCard | 100.011.091 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C10H15Br | |
| Molar mass | 215.134 g·mol−1 | 
| Appearance | Solid | 
| Melting point | 117 °C (243 °F) | 
| Boiling point | 226 °C (439 °F) | 
| Insoluble | |
| Hazards | |
| NFPA 704 (fire diamond) | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
References
    
-  Reuben D. Rieke, Tse-Chong Wu, Loretta I. Rieke (1995). "Highly Reactive Calcium for the Preparation of Organocalcium Reagents: 1-Adamantyl Calcium Halides and Their Addition to Ketones: 1-(1-Adamantyl)cyclohexanol". Organic Syntheses. 72: 147. doi:10.15227/orgsyn.072.0147.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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