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