3-Iodophenol
Chemical compound
From Wikipedia, the free encyclopedia
3-Iodophenol (m-iodophenol) is an aromatic organic compound. 3-Iodophenol participates in a variety of coupling reactions in which the iodide substituent is displaced.[4] Well cited examples include thiolate[5] and amine nucleophiles.[6]
| Names | |
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| IUPAC name
3-Iodophenol | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.009.931 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H5IO | |
| Molar mass | 220.009 g·mol−1 |
| Melting point | 118 °C (244 °F; 391 K)[1] |
| Boiling point | 186 °C (367 °F; 459 K)[1] (100 mmHg) |
| Acidity (pKa) | 9.03[2] |
| Hazards | |
| GHS labelling:[3] | |
| Warning | |
| H315, H319, H335 | |
| P261, P305+P351+P338 | |
| Related compounds | |
Related compounds |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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3-Iodophenol can be prepared by oxidative decarboxylation of 3-iodobenzoic acid:[7]
- IC6H4CO2H + "O" → IC6H4OH + CO2
