Iodocyclopropane
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Names | |
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Preferred IUPAC name
Iodocyclopropane | |
Other names
Cyclopropyl iodide, cyclopropyliodide
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
EC Number |
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PubChem CID
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Properties | |
C3H5I | |
Molar mass | 167.977 g·mol−1 |
Appearance | Liquid |
Density | g/cm3 |
Hazards | |
GHS labelling: | |
H315, H319, H335 | |
Related compounds | |
Related compounds
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Fluorocyclopropane Bromocyclopropane Chlorocyclopropane |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Iodocyclopropane is a organoiodine compound with the chemical formula C3H5I.[1][2] The compound is a member of haloalkane family.
Chemical properties
The compound reacts with benzoxazole to produce 2-cyclopropylbenzoxazole in presence of palladium catalyst.[3]
Uses
Iodocyclopropanes are used as synthetic intermediates to synthesize many alkyl, aryl, and acyl substituted cyclopropanes via organometallic reactions.[4]
See also
References
- ^ "Iodocyclopropane". Manchester Organics. Retrieved 31 May 2023.
- ^ "Iodocyclopropane". Sigma Aldrich. Retrieved 31 May 2023.
- ^ Wu, Xiaojin; Lei, Chuanhu; Yue, Guizhou; Zhou, Jianrong Steve (10 August 2015). "Palladium-Catalyzed Direct Cyclopropylation of Heterocycles". Angewandte Chemie International Edition. 54 (33): 9601–9605. doi:10.1002/anie.201504735. hdl:10356/89367. PMID 26179255.
- ^ Martin, Stephen F.; Dwyer, Michael P. (19 March 1998). "Iodocyclopropanes as versatile intermediates for the synthesis of substituted cyclopropanes". Tetrahedron Letters. 39 (12): 1521–1524. doi:10.1016/S0040-4039(98)00072-0. ISSN 0040-4039. Retrieved 31 May 2023.
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- Cyclopropanes
- Iodine compounds
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