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]

Quick facts Names, Identifiers ...
3-Iodophenol
Names
IUPAC name
3-Iodophenol
Other names
    • m-Iodophenol
    • meta-Iodophenol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.009.931 Edit this at Wikidata
EC Number
  • 210-923-2
UNII
  • InChI=1S/C6H5IO/c7-5-2-1-3-6(8)4-5/h1-4,8H
    Key: FXTKWBZFNQHAAO-UHFFFAOYSA-N
  • C1=CC(=CC(=C1)I)O
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]
GHS07: Exclamation mark
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).
Close

3-Iodophenol can be prepared by oxidative decarboxylation of 3-iodobenzoic acid:[7]

IC6H4CO2H + "O" → IC6H4OH + CO2

References

Cited sources

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