CAS 18711-13-2
:4,7-Dichlorisatin
- 1H-Indole-2,3-dione, 4,7-dichloro-
- 4,7-Dichloroindoline-2,3-dione
- 4,7-dichloro-1H-indole-2,3-dione
- Indole-2,3-dione, 4,7-dichloro-
- Isatin, 4,7-dichloro-
- 4,7-Dichloroisatin
- BUTTPARK 50\07-81
4,7-Dichloroisatin, 98%
CAS: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 part of the brand transition to Thermo Sci
Formel:C8H3Cl2NO2Reinheit:98%Farbe und Form:Powder, OrangeMolekulargewicht:216.024,7-Dichloroindoline-2,3-dione
CAS:Formel:C8H3Cl2NO2Reinheit:95%Farbe und Form:SolidMolekulargewicht:216.02094,7-Dichloroisatin
CAS:4,7-DichloroisatinReinheit:≥95%Farbe und Form:Orange-Brown PowderMolekulargewicht:216.02g/mol4,7-Dichloroisatin
CAS:4,7-Dichloroisatin is an organic compound that is synthesized by ring-opening of oxindole. It is a bifunctional molecule that can be used for the synthesis of other organic compounds. 4,7-Dichloroisatin has been found to be an efficient method for the synthesis of thiazolidinedione derivatives and can be used as a control experiment for this type of reaction. The mechanism for the reaction includes nitroaldol addition to the C=O group, followed by nucleophilic attack on the carbonyl group to form a tetrahedral intermediate. The intermediate then collapses to form a new C=N bond and release acetonitrile.
Formel:C8H3Cl2NO2Reinheit:Min. 95%Farbe und Form:SolidMolekulargewicht:216.02 g/mol




