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N-Cyclohexylmaleimide

Basic information Safety Supplier Related

N-Cyclohexylmaleimide Basic information

Product Name:
N-Cyclohexylmaleimide
Synonyms:
  • 2-amino-4-(2-chlorophenyl)-3-thiophenecarboxylic acid methyl ester
  • Cyclohexylmaleimide
  • 1H-Pyrrole 2,5-Dione ,1-Cyclohexyl
  • ChemicalbookTIMTEC-BBSBB005910
  • N-CYCLOHEXYLMALEIC IMIDE
  • N-CYCLOHEXYLMALEIMIDE
  • TIMTEC-BB SBB005910
  • ASISCHEM D13289
CAS:
1631-25-0
MF:
C10H13NO2
MW:
179.22
EINECS:
216-630-6
Product Categories:
  • Intermediates of Dyes and Pigments
  • N-Substituted Maleimides
  • N-Substituted Maleimides, Succinimides & Phthalimides
  • Carbonyl Compounds
  • Cyclic Imides
  • Organic Building Blocks
Mol File:
1631-25-0.mol
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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
form 
powder to lump
pka
-2.26±0.20(Predicted)
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)
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Safety Information

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

MSDS

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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

Not classified

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