ChemicalBook--->CAS DataBase List--->84661-56-3

84661-56-3

84661-56-3 Structure

84661-56-3 Structure
IdentificationBack 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
[MDL Number]

MFCD00159695
[MOL File]

84661-56-3.mol
[Molecular Weight]

148.17
Chemical PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

N,N-diimidazoylmethane(84661-56-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Imidazole

288-32-4

Dichloromethane

75-09-2

N,N-diimidazoylmethane

84661-56-3

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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