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ChemicalBook >  Product Catalog >  Organic Chemistry >  Nitrogen Compounds >  2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile

2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile

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2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile Basic information

Product Name:
2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile
Synonyms:
  • 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile
  • 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)propanedinitrile
  • (3 5 5-TRIMETHYLCYCLOHEX-2-ENYLIDENE)MA&
  • (3,5,5-trimethyl-2-cyclohexen-1-ylidene)-propanedinitril
  • (3,5,5-trimethyl-2-cyclohexen-1-ylidene)propanedinitrile
  • 3-dicyanomethylene-1,5,5-trimethylcyclohexene
  • Propanedinitrile, 2-(3,5,5-trimethyl-2-cyclohexen-1-ylidene)-
CAS:
23051-44-7
MF:
C12H14N2
MW:
186.25
Product Categories:
  • Monomers
  • Polymer Science
  • Vinyl Halides, Amines, Amides, and Other Vinyl Monomers
Mol File:
23051-44-7.mol
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2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile Chemical Properties

Melting point:
73-77 °C (lit.)
Boiling point:
175-176 °C(Press: 19 Torr)
Density 
1.007±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
color 
White to Light yellow powder to crystal
EPA Substance Registry System
Propanedinitrile, (3,5,5-trimethyl-2-cyclohexen-1-ylidene)- (23051-44-7)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-43
Safety Statements 
36/37
WGK Germany 
3
RTECS 
TY1590000
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2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile Usage And Synthesis

Synthesis

In a 100?mL round bottom flask, isophorone 3.45 g (25 mmol) and malononitrile 1.65 g (25 mmol) were dissolved in anhydrous ethanol 50 mL. Then sodium acetate trihydrate (1g, 12.5mmol) was added. The mixture was heated to 80°C and stirred for about 12h. The reaction progress was monitored by TLC. Once the starting isophorone disappeared on TLC and the target spot formed regularly, the reaction mixture was cooled to room temperature. The solid sodium acetate trihydrate was removed by filtration. 25mL Ethanol was removed in a vacuum. The left mixture stood still at 27°C overnight. The crystals were collected by filtration and washed carefully with cooled anhydrous ethanol. 2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile can be obtained by recrystallization one more time from ethanol.

Structure and conformation

2-(3,5,5-trimethylcyclohex-2-en-1-ylidene)malononitrile (C12H14N2), monoclinic, P21/c (no. 14), a = 10.16290(10)Å, b = 8.25800(10)Å, c = 13.4328(2), β = 95.910(1)°, V = 1121.36(2)Å3, Z = 4, R gt (F) = 0.0380, wR ref (F2) = 0.1126, T = 294 K.

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