3-Iodophenol
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| Names | |
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| IUPAC name
3-Iodophenol
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Other names
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| EC Number |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
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)[2] |
| Boiling point | 186 °C (367 °F; 459 K)[2] (100 mmHg) |
| Acidity (pKa) | 9.03[1] |
| Hazards | |
| GHS labelling:[3] | |
| GHS07: Exclamation mark | |
| 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 (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]
3-Iodophenol can be prepared by oxidative decarboxylation of 3-iodobenzoic acid:[7]
- IC6H4CO2H + "O" → IC6H4OH + CO2
References
[edit | edit source]- ^ Haynes, p. 5.93
- ^ a b Haynes, p. 3.324
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Cited sources
[edit | edit source]- Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
