| Identification | More | [Name]
N-Cyclohexylmaleimide | [CAS]
1631-25-0 | [Synonyms]
1-CYCLOHEXYL-1H-PYRROLE-2,5-DIONE
1-CYCLOHEXYL-PYRROLE-2,5-DIONE
AKOS MSC-0038
ASISCHEM D13289
N-CYCLOHEXYLMALEIC IMIDE
N-CYCLOHEXYLMALEIMIDE
TIMTEC-BB SBB005910
N-Cyclohexylmaleinimide
1-Cyclohexyl-3-pyrroline-2,5-dione | [EINECS(EC#)]
216-630-6 | [Molecular Formula]
C10H13NO2 | [MDL Number]
MFCD00043904 | [Molecular Weight]
179.22 | [MOL File]
1631-25-0.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
2811 | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [TSCA ]
Yes | [HazardClass ]
6.1 | [PackingGroup ]
II | [HS Code ]
29251900 |
| Hazard Information | Back Directory | [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 |
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