Informations sur le produit
- N-hydroxyphthalimide
- 1H-Isoindole-1,3(2H)-dione, 2-hydroxy-
- 2-Hydroxy-2,3-dihydro-1H-isoindole-1,3-dione
- 2-Hydroxyisoindole-1,3-dione
- 2-Hydroxyisoindoline-1,3-dione
- 2-Hydroxyphthalimide
- 2-hydroxy-1H-isoindole-1,3(2H)-dione
- F 802
- N-Hydroxyphtalimide
- N-Hydroxyphthalamide
- Voir d'autres synonymes
- N-Hydroxyphthalimde
- N-Hydroxyphthalimid
- N-Hydroxyphthalimide
- N-hidroxiftalimida
- Nsc 770
- Phthalimide, N-Hydroxy-
Aerobic oxidation of various alcohols has been accomplished by using a new catalytic system, N-hydroxyphthalimide (NHPI) combined with Co (acac). A practical catalytic method to convert alkylbenzenes into the corresponding carboxylic acids under atmospheric dioxygen at ambient temperature using a combined catalytic system consisting of N-hydroxyphthalimide (NHPI) and Co (OAc) 2 was developed. Novel catalysis by N-hydroxyphthalimide in the oxidation of organic substrates by molecular oxygen was described. Free radical functionalization of organic compounds catalyzed by N-hydroxyphthalimide. Purely organic and catalytic systems of anthraquinones and N-hydroxyphthalimide efficiently promote oxygenation of hydrocarbons with dioxygen under mild conditions. Hydroxylation of polycyclic alkanes with molecular oxygen catalyzed by N-hydroxyphthalimide (NHPI) combined with was transition metal salts. 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.
Propriétés chimiques
Question d’ordre technique sur : 02-A13862 N-Hydroxyphthalimide, 98+%
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