CAS 80360-14-1
:3-Iodo-1-(fenilsulfonil)indol
- 1H-indole, 3-iodo-1-(phenylsulfonyl)-
- 3-Iodo-1-(phenylsulfonyl)-1H-indole
3-Iodo-1-(phenylsulfonyl)indole, 95%
CAS:It is used as pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a
Fórmula:C14H10INO2SPureza:95%Forma y color:Pale cream to cream, PowderPeso molecular:383.23-Iodo-1-(phenylsulfonyl)-1H-indole
CAS:Fórmula:C14H10INO2SPureza:97%Forma y color:SolidPeso molecular:383.20423-Iodo-1-(phenylsulfonyl)-1H-indole
CAS:3-Iodo-1-(phenylsulfonyl)-1H-indolePureza:97%Peso molecular:383.20g/mol3-Iodo-1-(phenylsulfonyl)-1H-indole
CAS:Fórmula:C14H10INO2SPureza:97%Forma y color:SolidPeso molecular:383.23-Iodo-1-(phenylsulfonyl)indole
CAS:3-Iodo-1-(phenylsulfonyl)indole (3-ISI) is a ligand that is used to crystallize metal ions. 3-ISI binds to metal ions through interactions with the halide ion. The 3-ISI molecule has two phenylsulfonyl groups and one iodine atom, which are the sites of coordination to metal ions. Friedel-Crafts acylation reactions use 3-ISI as a ligand because it does not react with the catalyst or acid, but can be easily replaced by other ligands during the reaction. Parameters for determining its structure include X-ray crystallography, NMR spectroscopy, IR spectroscopy, and elemental analysis. The chloride anion in 3-ISI is able to form hydrogen bonds with other chloride anions in order to stabilize its structure.
3-ISI can be synthesized by reacting iodides with benzyl bromide and phosphorous pentFórmula:C14H10INO2SPureza:Min. 95%Peso molecular:383.21 g/molRef: 3D-FDA36014
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