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Chemical Structure| 21149-98-4 Chemical Structure| 21149-98-4

Structure of 21149-98-4

Chemical Structure| 21149-98-4

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Product Details of [ 21149-98-4 ]

CAS No. :21149-98-4
Formula : C7H12N2
M.W : 124.18
SMILES Code : CC(C1=CNC=N1)(C)C
MDL No. :MFCD18064644

Safety of [ 21149-98-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 21149-98-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 21149-98-4 ]

[ 21149-98-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4761-00-6 ]
  • [ 21149-98-4 ]
  • 4-tert-butyl-1-[(2,4,6-trimethylphenyl)methyl]-1H-imidazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% With caesium carbonate; In acetonitrile; at 20℃; To 4-ten-butyl-1H-imidazole (1.37 g, 11.0 mmol) and cesium carbonate (7.20 g, 22.0 mmol) in acetonitrile (24 mL) was added 2-(bromomethyl)-1,3,5-trimethyl benzene (1.58 g, 9.38 mmol). The resulting suspension was stirred at room temperature overnight. Heptane (10 mL) was added to the reaction mixture before it was filtered through a pad of silica and washed with a 1:1 mixture of ethyl acetate:heptane. The eluent was concentrated to provide 4-tert-butyl-1-[(2,4,6-trimethylphenyl)methyl]-1H-imidazole (1.47 g, 52%) as an oil. 1H NMR (300 MHz, DMSO) delta 1.15 (s, 9H), 2.26 (s, 6H), 2.29 (s, 3H), 5.02 (s, 2H), 6.43 (s, 1H), 6.90 (s, 2H), 7.23 (s, 1H).
 

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