194115
4-Chlorophenyl phenyl sulfone
≥97%
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About This Item
Linear Formula:
ClC6H4SO2C6H5
CAS Number:
Molecular Weight:
252.72
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-242-1
MDL number:
Assay:
≥97%
assay
≥97%
mp
90-94 °C (lit.)
solubility
acetone: soluble 74.4 g/100ml at 20 °C(lit.), benzene: soluble 44.4 g /100ml at 20 °C(lit.), dioxane: soluble 65.6 g/100ml at 20 °C(lit.), hexane: soluble 0.4 g/100ml at 20 °C(lit.), isopropanol: soluble 21 g/100ml at 20 °C(lit.)
functional group
chloro, sulfone
SMILES string
Clc1ccc(cc1)S(=O)(=O)c2ccccc2
InChI
1S/C12H9ClO2S/c13-10-6-8-12(9-7-10)16(14,15)11-4-2-1-3-5-11/h1-9H
InChI key
OFCFYWOKHPOXKF-UHFFFAOYSA-N
General description
4-Chlorophenyl phenyl sulfone is also referred to as sulphenone. It participates in palladium-catalyzed amidation reaction in the presence of low CO pressures and an iodide salt.
Application
4-Chlorophenyl phenyl sulfone was employed in polyetherification reaction of 4,4′-dihalodiphenyl sulfones.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Robert J. Perry et al.
The Journal of organic chemistry, 61(21), 7482-7485 (1996-10-18)
The palladium-catalyzed amidation of electron-deficient aryl chlorides proceeds readily in the presence of low CO pressures and a slight excess of an iodide salt. The rates of amidation are accelerated over those without added salt, and iodide is preferred over
Reductive dehalogenation versus substitution in the polyetherification of 4, 4'-dihalodiphenyl sulfones with bisphenolates.
Percec V, et al.
Macromolecules, 26(14), 3650-3662 (1993)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 194115-100G | 04061832418803 |