Chloroiodomethane
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| Names | |
|---|---|
|  Preferred IUPAC name
 Chloroiodomethane  | |
|  Systematic IUPAC name
 Chloro(iodo)methane[1]  | |
 Other names
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| Identifiers | |
|  593-71-5  | |
| 1730802 | |
| ChemSpider |  11154  | 
| EC Number | 209-804-8 | 
| Jmol interactive 3D | Image | 
| PubChem | 11644 | 
 
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| Properties | |
| CH2ClI | |
| Molar mass | 176.38 g·mol−1 | 
| Appearance | Colorless liquid | 
| Density | 2.422 g mL−1 | 
| Boiling point | 108 to 109 °C (226 to 228 °F; 381 to 382 K) | 
|   Henry's law constant (kH)  | 
8.9 μmol Pa−1 kg−1 | 
|   Refractive index (nD)  | 
1.582 | 
| Hazards | |
| GHS pictograms |  ![]()  | 
| GHS signal word | WARNING | 
| H315, H319, H335 | |
| P261, P305+351+338 | |
|   EU classification (DSD)  | 
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| R-phrases | R36/37/38 | 
| S-phrases | S26, S36 | 
| NFPA 704 | |
| Related compounds | |
|   Related alkanes  | 
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|   Related compounds  | 
2-Chloroethanol | 
|   Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  | |
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| Infobox references | |
Chloroiodomethane is a mixed liquid halomethane very soluble in acetone, benzene, diethyl ether and alcohol. Its refractive index is 1.5812 - 1.5832.
It crystallizes orthorhombic crystal system with space group Pnma with lattice constants: a = 6.383, b = 6.706, c = 8.867 (.10−1 nm).[2]
Chloroiodomethane is used in cyclopropanation (Simmon-Smith reaction), Mannich reaction, aminomethylation, epoxidation, ring opening and addition to terminal alkenes. It often replaces diiodomethane because of higher yields and selectivity.
References
- ↑ "CHLOROIODOMETHANE - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 27 March 2005. Identification. Retrieved 23 June 2012.
 - ↑ Torrie B. H. ; Binbrek O. S.; von Dreele R. (1993). "Crystal structure of chloroiodomethane". Mol. Phys. 79 (4): 869–874(6). doi:10.1080/00268979300101691. Retrieved 2007-06-29.
 
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