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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 |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAA1386222
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Thermo Scientific Chemicals
A1386222 |
100 g |
Each for $78.92
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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.
ApplicationsAerobic 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.
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% |
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
RUO – Research Use Only