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| | N-Cyclohexylmaleimide Basic information |
| | N-Cyclohexylmaleimide Chemical Properties |
| Melting point | 89-91 °C (lit.) | | Boiling point | 132 °C / 17mmHg | | density | 1.226±0.06 g/cm3(Predicted) | | vapor pressure | 80Pa at 25℃ | | storage temp. | Inert atmosphere,Room Temperature | | solubility | Insoluble in water | | pka | -2.26±0.20(Predicted) | | form | powder to lump | | color | White to Almost white | | Water Solubility | 260mg/L at 25℃ | | LogP | 2.57 at 23℃ | | CAS DataBase Reference | 1631-25-0(CAS DataBase Reference) | | EPA Substance Registry System | 1H-Pyrrole-2,5-dione, 1-cyclohexyl- (1631-25-0) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-37/39 | | RIDADR | 2811 | | WGK Germany | 3 | | Hazard Note | Irritant | | TSCA | Yes | | HazardClass | 6.1 | | PackingGroup | II | | HS Code | 29251900 |
| | N-Cyclohexylmaleimide Usage And Synthesis |
| Uses | N-Cyclohexylmaleimide (CHMI, NCMI) may be used for the preparation of hyperbranched copolymers of p-(chloromethyl)styrene (CMS) and NCMI, via atom transfer radical copolymerization reaction. | | Synthesis Reference(s) | Synthetic Communications, 20, p. 1607, 1990 DOI: 10.1080/00397919008053079 | | General Description | N-Cyclohexylmaleimide (CHMI, NCMI) is a cyclic imide. Diels-Alder reactions of 9-hydroxymethylanthracene with CHMI catalyzed by hydrophobic nanospace confined within the self-assembled Pd6 open cage bearing triimidazole walls have been reported. It undergoes Diels-Alder reactions with various aromatic hydrocarbons promoted by self-assembled coordination cage. This cage acts as nanometer-sized molecular flask and hence promotes this reaction. CHMI is reported to undergo radical polymerization readily under various polymerization conditions to afford poly(CHMI), having excellent thermal stability. | | Flammability and Explosibility | Notclassified |
| | N-Cyclohexylmaleimide Preparation Products And Raw materials |
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