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N-Hydroxyphthalimide, 98%

Code produit 11471528
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Code produit 11471528 Fournisseur Thermo Scientific Alfa Aesar Code fournisseur A13862.36
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Estimated Shipment: 24-11-2026
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CAS: 524-38-9 | C8H5NO3 | 163.13 g/mol

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.

Applications
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.

Solubility
Slightly soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
TRUSTED_SUSTAINABILITY

Identifiants chimiques

CAS 524-38-9
Molecular Formula C8H5NO3
Molecular Weight (g/mol) 163.13
MDL Number MFCD00005891
InChI Key CFMZSMGAMPBRBE-UHFFFAOYSA-N
Synonym n-hydroxyphthalimide, 2-hydroxyisoindoline-1,3-dione, 2-hydroxy-1h-isoindole-1,3 2h-dione, nhpi, 2-hydroxyphthalimide, 1h-isoindole-1,3 2h-dione, 2-hydroxy, phthalimide, n-hydroxy, phthaloxime, unii-bxi99m81x0, 2-hydroxyisoindolin-1,3-dione
PubChem CID 10665
IUPAC Name 2-hydroxyisoindole-1,3-dione
SMILES ON1C(=O)C2=CC=CC=C2C1=O

Spécification

Melting Point ∼233°C (decomposition)
Quantity 500 g
Beilstein 131208
Merck Index 14,4838
Solubility Information Slightly soluble in water.
Formula Weight 163.13
Percent Purity ≥98%
Chemical Name or Material N-Hydroxyphthalimide

RUO – Research Use Only

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