| Weight | 111.1 g/mol |
|---|---|
| Formula | C5H5NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
N-Methylmaleimide (930-88-1)
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- Sigma-Aldrich - N-Methylmaleimide59.60 - 155.00 USD
- Fisher Scientific - Search for N-Methylmaleimide
- TCI - N-Methylmaleimide106.00 - 989.00 USD
- The Elusive Antiaromaticity of Maleimides and Maleic Anhydride: Enthalpies of Formation of N-Methylmaleimide, N-Methylsuccinimide, N-Methylphthalimide, and N-Benzoyl-N-methylbenzamide. (Journal of Organic Chemistry, 1997)
- FT-IR. FT-Raman, NMR spectra, and molecular structure investigation of 2,3-dibromo-N-methylmaleimide : A combined experimental and theoretical study (Journal of Molecular Structure, 2008)
- Structural studies on cycloadducts of furan, 2-methoxyfuran, and 5-trimethylsilylcyclopentadiene with maleic anhydride and N-methylmaleimide. (Journal of Organic Chemistry, 2008)
- A new class of transparent polymeric materials. I. Production and properties of an alternating copolymer of Nmethylmaleimide and isobutene (Journal of Applied Polymer Science, 1996)
- Asymmetric Base-Catalyzed Diels-Alder Reaction of 3-Hydroxy-2-Pyrone with N-Methylmaleimide (Chemistry Letters, 1996)
- Unusual stability of N-methylmaleimide cycloadducts : characterization of isobenzofuran retro-Diels-Alder reactions (Journal of Organic Chemistry, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C(=O)C=CC1=O
-
InChIKeySEEYREPSKCQBBF-UHFFFAOYSA-N
- Pubchem - N-Methylmaleimide
- Wikipedia - N-methylmaleimide
N-Methylmaleimide is a naturally-occurring organic compound with the formula of C5H5NO2.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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N-Methylmaleimide
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