CAS 18711-13-2: 4,7-Dichloroisatin
Formula:C8H3Cl2NO2
InChI:InChI=1S/C8H3Cl2NO2/c9-3-1-2-4(10)6-5(3)7(12)8(13)11-6/h1-2H,(H,11,12,13)
InChI key:InChIKey=NUXYYWOWNFEMNH-UHFFFAOYSA-N
SMILES:O=C1C=2C(=C(Cl)C=CC2Cl)NC1=O
Synonyms:- 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
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Found 5 products.
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 Scientific Chemicals.Formula:C8H3Cl2NO2Purity:98%Color and Shape:Powder, OrangeMolecular weight:216.024,7-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.Formula:C8H3Cl2NO2Purity:Min. 95%Color and Shape:SolidMolecular weight:216.02 g/mol4,7-Dichloroisatin
CAS:4,7-DichloroisatinColor and Shape:Orange-Brown PowderMolecular weight:216.02g/mol4,7-Dichloroindoline-2,3-dione
CAS:Formula:C8H3Cl2NO2Purity:95%Color and Shape:SolidMolecular weight:216.02092000000002
