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N-Hydroxyphthalimide, 98%

CAS: 524-38-9 | C8H5NO3 | 163.13 g/mol

$78.92 - $78.92

Chemical Identifiers

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
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AAA1386222
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Thermo Scientific Chemicals
A1386222
100 g
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Description

Description

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.
Specifications

Chemical Identifiers

524-38-9
163.13
CFMZSMGAMPBRBE-UHFFFAOYSA-N
10665
ON1C(=O)C2=CC=CC=C2C1=O
C8H5NO3
MFCD00005891
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
2-hydroxyisoindole-1,3-dione

Specifications

524-38-9
C8H5NO3
100 g
14,4838
Slightly soluble in water.
ON1C(=O)C2=CC=CC=C2C1=O
163.13
163.13
N-Hydroxyphthalimide
∼233°C (decomposition)
MFCD00005891
131208
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
CFMZSMGAMPBRBE-UHFFFAOYSA-N
2-hydroxyisoindole-1,3-dione
10665
≥98%
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

EINECSNumber : 208-358-1

RTECSNumber : TI5200000

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only