4-Iodophenol (p-iodophenol) is an aromatic organic compound. A colorless solid, it is one of three monoiodophenols. 4-Iodophenol undergoes a variety of coupling reactions in which the iodine substituent is replaced by a new carbon group para to the hydroxy group of the phenol.[3] It is also used to enhance chemiluminescence for detection of cancer cells[4] and in the Eclox assay.
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| Names | |
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| IUPAC name
4-Iodophenol
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Other names
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
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| DrugBank | |
| ECHA InfoCard | 100.007.951 |
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C6H5IO | |
| Molar mass | 220.009 g·mol−1 |
| Density | 1.8573 g/cm3 (112 °C)[1] |
| Melting point | 93.5 °C (200.3 °F; 366.6 K)[1] |
| Boiling point | 139 °C (282 °F; 412 K)[1] (5 mmHg; decomposes) |
| Acidity (pKa) | 9.33[2] |
| Hazards | |
| GHS labelling: | |
  [3]
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| H302, H312, H314 | |
| P280, P305+P351+P338, P310 | |
| 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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4-Iodophenol can be prepared from 4-aminophenol via the diazonium salt. An alternative synthesis involves reaction of salicylic acid with iodine, followed by decarboxylation.[5]
References edit
- ^ a b c Haynes, p. 3.324
- ^ Haynes, p. 5.93
- ^ a b "4-Iodophenol". Sigma-Aldrich.
- ^ "4-Iodophenol". Fisher Scientific.
- ^ Dains, F. B.; Eberly, Floyd (1935). "p-Iodophenol". Organic Syntheses. 15: 39. doi:10.15227/orgsyn.015.0039.
Cited sources edit
- Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. ISBN 9781498754293.
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