Identification | Back Directory | [Name]
N,N-diimidazoylmethane | [CAS]
84661-56-3 | [Synonyms]
N,N-diimidazoylmethane Di(1H-iMidazol-1-yl)Methane 1,1'-methylenebis-1H-Imidazole 1H-Imidazole, 1,1'-methylenebis- 1-(imidazol-1-ylmethyl)imidazole 1-(1H-iMidazol-1-ylMethyl)-1H-iMidazole | [Molecular Formula]
C7H8N4 | [MOL File]
84661-56-3.mol | [Molecular Weight]
148.17 |
Chemical Properties | Back Directory | [Melting point ]
168-169 °C(Solv: chloroform (67-66-3); methanol (67-56-1)) | [Boiling point ]
439.4±28.0 °C(Predicted) | [density ]
1.24±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [pka]
6.80±0.12(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
Potassium hydroxide (4.94 g, 88 mmol) was added to a stirred solution of imidazole (3.0 g, 44 mmol) in 100 mL of dichloromethane. The reaction mixture was refluxed at 50 °C for 12 hours. Upon completion of the reaction, the solvent was removed by decantation and the volatiles were removed by rotary evaporation to give the crude product of 1,1-methylenebis(imidazole). The crude product was washed with ether and dried to give a white solid. The final product was bis(1H-imidazol-1-yl)methane in the form of a white powder with a yield of 3.82 g in 60% yield. | [References]
[1] Heterocycles, 1992, vol. 34, # 7, p. 1365 - 1373 [2] Journal of Heterocyclic Chemistry, 1983, vol. 20, p. 1245 - 1249 [3] Journal of Heterocyclic Chemistry, 2017, vol. 54, # 6, p. 3065 - 3070 [4] Organometallics, 2017, vol. 36, # 17, p. 3250 - 3256 [5] Journal of Coordination Chemistry, 2013, vol. 66, # 18, p. 3211 - 3228 |
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