Names | |
---|---|
IUPAC name
2-Iodophenol
| |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.007.792 |
EC Number |
|
406034 | |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H5IO | |
Molar mass | 220.009 g·mol−1 |
Density | 1.8757 g/cm3 (80 °C) [1] |
Melting point | 43 °C (109 °F; 316 K) [1] |
Boiling point | 186 °C (367 °F; 459 K) [1] (160 mmHg) |
Acidity (pKa) | 8.51 [2] |
Hazards | |
GHS labelling: | |
[3] | |
H302, H312, H315, H319, H332, H335 | |
P261, P280, 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).
|
2-Iodophenol (o-iodophenol) is an aromatic organic compound with the formula IC6H4OH. It is a pale yellow solid that melts near room temperature. It undergoes a variety of coupling reactions in which the iodine substituent is replaced by a new carbon group ortho to the hydroxy group of the phenol, which can be followed by cyclization to form heterocycles. [3]
It can be prepared by treatment of 2-chloromercuriphenol with iodine:
Direct reaction of phenol with iodine gives a mixture of 2- and 4-iodo derivatives. [4]
Names | |
---|---|
IUPAC name
2-Iodophenol
| |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.007.792 |
EC Number |
|
406034 | |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H5IO | |
Molar mass | 220.009 g·mol−1 |
Density | 1.8757 g/cm3 (80 °C) [1] |
Melting point | 43 °C (109 °F; 316 K) [1] |
Boiling point | 186 °C (367 °F; 459 K) [1] (160 mmHg) |
Acidity (pKa) | 8.51 [2] |
Hazards | |
GHS labelling: | |
[3] | |
H302, H312, H315, H319, H332, H335 | |
P261, P280, 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).
|
2-Iodophenol (o-iodophenol) is an aromatic organic compound with the formula IC6H4OH. It is a pale yellow solid that melts near room temperature. It undergoes a variety of coupling reactions in which the iodine substituent is replaced by a new carbon group ortho to the hydroxy group of the phenol, which can be followed by cyclization to form heterocycles. [3]
It can be prepared by treatment of 2-chloromercuriphenol with iodine:
Direct reaction of phenol with iodine gives a mixture of 2- and 4-iodo derivatives. [4]