Chloroiodomethane
Names | |
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Preferred IUPAC name
Chloroiodomethane | |
Systematic IUPAC name
Chloro(iodo)methane[1] | |
Other names
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Identifiers | |
1730802 | |
593-71-5 | |
ChemSpider | 11154 |
EC number | 209-804-8 |
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Jmol-3D images | Image |
PubChem | 11644 |
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Properties | |
Molecular formula |
CH2ClI |
Molar mass | 176.38 g·mol−1 |
Appearance | Colorless liquid |
Density | 2.422 g mL−1 |
Boiling point | 108 °C (226 °F; 381 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 | Xi |
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 noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
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.
External links
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