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) [2] |
Boiling point | 186 °C (367 °F; 459 K) [2] (100 mmHg) |
Acidity (pKa) | 9.03 [1] |
Hazards | |
GHS labelling: [3] | |
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).
|
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]
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) [2] |
Boiling point | 186 °C (367 °F; 459 K) [2] (100 mmHg) |
Acidity (pKa) | 9.03 [1] |
Hazards | |
GHS labelling: [3] | |
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).
|
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]