| Weight | 187.198 g/mol |
|---|---|
| Formula | C11H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
N-Benzylmaleimide (1631-26-1)
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- Iridium-catalyzed double incorporation reaction of N-benzylmaleimide to styrene via ortho-CH bond activation, initiated by precoordination of the double bond of styrene to iridium (Tetrahedron Letters, 2005)
- Copolymerization of optically active N-(l-menthoxycarbonylmethyl)maleimide with N-phenyl- or N-benzylmaleimide (Polymer, 1995)
- Development of Multikilogram Continuous Flow Cyclopropanation of N-Benzylmaleimide through Kinetic Analysis (Organic Process Research & Development, 2014)
- Synthesis and properties of sulfonated poly(phosphazene)graftpoly(styrenecoNbenzylmaleimide) copolymers via atom transfer radical polymerization for proton exchange membrane (Journal of Applied Polymer Science, 2015)
- Reaction of functionalized pyrone with N-benzylmaleimide: study of the relevant parameters for isolation of cycloadducts (Designed Monomers and Polymers, 2006)
- STUDIES IN RADIATION POLYMERIZATION. XV. THE RADIATION POLYMERIZATION OF N-BENZYLMALEIMIDE. (1970)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)CN2C(=O)C=CC2=O
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InChIKeyMKRBAPNEJMFMHU-UHFFFAOYSA-N
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