| Weight | 163.132 g/mol |
|---|---|
| Formula | C8H5NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
N-HYDROXYPHTHALIMIDE (524-38-9)
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#92 in Physical chemistry
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#2205 in Physics
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#6817 in Chemistry
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- Free Radical Functionalization of Organic Compounds Catalyzed by N-Hydroxyphthalimide (Chemical Reviews, 2007)
- Alkane Oxidation with Molecular Oxygen Using a New Efficient Catalytic System: N-Hydroxyphthalimide (NHPI) Combined with Co(acac)n (n = 2 or 3) (Journal of Organic Chemistry, 1996)
- Novel Catalysis by N-Hydroxyphthalimide in the Oxidation of Organic Substrates by Molecular Oxygen (Journal of Organic Chemistry, 1995)
- Catalytic Oxidation of Alkylbenzenes with Molecular Oxygen under Normal Pressure and Temperature by N-Hydroxyphthalimide Combined with Co(OAc)2 (Journal of Organic Chemistry, 1997)
- Efficient Oxidation of Alcohols to Carbonyl Compounds with Molecular Oxygen Catalyzed by N-Hydroxyphthalimide Combined with a Co Species (Journal of Organic Chemistry, 2000)
- PdCl2 and NHydroxyphthalimide Cocatalyzed C sp 2H Hydroxylation by Dioxygen Activation (Angewandte Chemie, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=O)N(C2=O)O
-
InChIKeyCFMZSMGAMPBRBE-UHFFFAOYSA-N
- Pubchem - N-HYDROXYPHTHALIMIDE
- Wikipedia - N-hydroxyphthalimide
N-Hydroxyphthalimide is the N-hydroxy derivative of phthalimide. The compound is used, inter alia, as catalyst for oxidation reactions, in particular for the selective oxidation (e. g.
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