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| Names | |
|---|---|
| Preferred IUPAC name Iodocyclohexane | |
| Other names Cyclohexyl iodide | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.009.962 
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| EC Number |
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| PubChem CID | |
| CompTox Dashboard (EPA) | |
InChI
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SMILES
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| Properties | |
| Chemical formula | C6H11I |
| Molar mass | 210.058 g·mol |
| Appearance | colorless to slightly reddish yellow liquid |
| Density | 1.624 g/mL |
| Boiling point | 180 °C (356 °F; 453 K) |
| Solubility in water | Insoluble |
| Hazards | |
| Flash point | 71 °C (160 °F; 344 K) |
| Related compounds | |
| Related compounds | Chlorocyclohexane Bromocyclohexane Fluorocyclohexane |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references | |
Iodocyclohexane is an organoiodine compound with the chemical formula C6H11I.
Synthesis
Iodocyclohexane has been prepared by the addition of hydrogen iodide to cyclohexene.
Alternatively, it can be prepared by the reaction of cyclohexane and iodoform.
Physical properties
Iodocyclohexane forms colorless to slightly reddish yellow liquid. It is soluble in ethanol, ether, and acetone.
Uses
The compound has been used as reagent in demethylation of aryl methyl ethers in DMF under reflux condition.
See also
References
- ^ "B24840 Iodocyclohexane, 98%, stab. with copper". Alfa Aesar. Retrieved 21 June 2023.
- "Iodocyclohexane". Sigma Aldrich. Retrieved 21 June 2023.
- Stone, Herman; Shechter, Harold (1951). "Iodocyclohexane". Organic Syntheses. 31: 66. doi:10.15227/orgsyn.031.0066.
- "Synthesis of iodocyclohexane from cyclohexane and iodoform" (PDF). oc-praktikum.de. Retrieved 21 June 2023.
| Iodine compounds | |
|---|---|
| Iodine(−I) | |
| Iodine(I) | |
| Iodine(II) | |
| Iodine(III) | |
| Iodine(IV) | |
| Iodine(V) | |
| Iodine(VII) | |