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| | 4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione Basic information |
| Product Name: | 4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione | | Synonyms: | 4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione;1H-Isoindole-1,3(2H)-dione, 4,5,6,7-tetrachloro-2-hydroxy-;3,4,5,6-Tetrachloro-N-hydroxyphthalimide;4,5,6,7-tetrachloro-2-hydroxy-2,3-dihydro-1H-isoin
dole-1,3-dione;4,5,6,7-tetrachloro-2-hydroxyisoindoline-1,3-dione;TCNHPI;N-Hydroxytetrachlorophthalimide | | CAS: | 85342-65-0 | | MF: | C8HCl4NO3 | | MW: | 300.91 | | EINECS: | | | Product Categories: | | | Mol File: | 85342-65-0.mol |  |
| | 4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione Chemical Properties |
| Boiling point | 532.1±60.0 °C(Predicted) | | density | 2.041±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | solubility | DMSO (Slightly), Methanol (Slightly) | | pka | 6.04±0.58(Predicted) | | form | Solid | | color | Light Yellow |
| | 4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione Usage And Synthesis |
| Uses | New reagent enabling the electrochemical allylic C-H oxidation reaction developed by the Baran group. This method provides a scalable and sustainable alternative to current strategies based on toxic reagents or precious metals. | | General Description | N-Hydroxytetrachlorophthalimide (TCNHPI) is an aryl-tetrahalogenated N-hydroxyphthalimide derivative. In combination with 1,4-diamino-2,3-dichloroanthraquinone (DADCAQ), it forms an efficient catalytic system for the oxidation of aromatic hydrocarbons using molecular oxygen under metal-free and aerobic conditions. | | reaction suitability | reagent type: oxidant |
| | 4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione Preparation Products And Raw materials |
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