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Chemical Structure| 32321-30-5 Chemical Structure| 32321-30-5

Structure of 32321-30-5

Chemical Structure| 32321-30-5

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Product Details of [ 32321-30-5 ]

CAS No. :32321-30-5
Formula : C12H20N2
M.W : 192.30
SMILES Code : CC1=C(CN)C(C)=C(C)C(CN)=C1C

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Application In Synthesis of [ 32321-30-5 ]

* 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 [ 32321-30-5 ]

[ 32321-30-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 628-36-4 ]
  • [ 32321-30-5 ]
  • 4-(4-((4H-1,2,4-triazol-4-yl)methyl)-2,3,5,6-tetramethyl-phenyl)-4H-1,2,4-triazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% at 150℃; for 24h; Equipped with a magnetic promoter, were added to the three 50mL round bottom flask with a reflux condenser and a thermometer (4- (aminomethyl) -2, 3,5,6-tetramethyl phenyl) methanamine (1 mmol of) and bis formic hydrazide (4mmol), stirring was started at 150Othe C, reacted for 24 hours.After completion of the reaction, the reaction solution was cooled to room temperature, the resulting precipitate was added to 100mL of hot methanol, and stirred to dissolve, filtered, and the filtrate was slowly volatilize give a white solid, yield 85percent.
85% at 150℃; for 24h; 4-(aminomethyl)-2,3,5,6-tetramethylphenylmethanamine: <strong>[628-36-4]N,N'-bisformylhydrazine</strong> molar ratio of 1:4Into a three-mouth round-bottom flask equipped with magnetic stirrer, reflux condenser and a thermometer were respectively added 4-(aminomethyl)-2,3,5,6-tetramethylphenylmethanamine (1mmol) and <strong>[628-36-4]N,N'-bisformylhydrazine</strong> (4mmol). Start the stirring at 150 deg.C. React for 24 hours. After the reaction, the reaction liquid to room temperature, will be precipitated by adding 100 ml hot methanol, after stirring to dissolve, filtered, filtrate slowly volatilized to obtain white solid, yield 85percent.
85% at 150℃; for 24h; In the provided with a magneton, reflux condenser and a thermometer of the 50 ml round bottom flask in three separately adding (4 - (aminomethyl) - 2, 3, 5, 6 - tetramethyl-phenyl) methylamine (1 mmol) and double-carbohydrazide (4 mmol), stir in 150oC, reaction 24 hours. After the reaction, the reaction liquid to room temperature, the obtained precipitation by adding 100 ml hot methanol, stirring to dissolve, filtering, the filtrate volatilize slow to get white solid, yield 85percent.The invention is preferably (4 - (aminomethyl) - 2, 3, 5, 6 - tetramethyl-phenyl) methylamine and double-carbohydrazide molar ratio of 1:4; the reaction temperature is 150 °C, the reaction time is 24 hours. The "one-pot", the (4 - (aminomethyl) - 2, 3, 5, 6 - tetramethyl-phenyl) methylamine and double-carbohydrazide under the heating condition for the preparation of 4 - (4 - ((4H - 1,2, 4 - triazole -4 - yl) methyl) - 2, 3, 5, 6 - tetramethyl-phenyl) - 4H - 1,2, 4 - triazole (L).
85% at 150℃; for 24h; (4- (aminomethyl) -2,3,5,6-tetramethylphenyl) methylamine:The molar ratio of bishydrazide is 1: 4(4- (aminomethyl) -2,3,5,6-tetramethylphenyl) methylamine (1 mmol) was added to a 50 mL three-necked round bottom flask equipped with a magnet, a reflux condenser and a thermometer, And dicarboxylic acid hydrazide (4 mmol)Start stirring at 150 oC,The reaction was carried out for 24 hours.After the reaction,The reaction solution was allowed to cool to room temperature,The resulting precipitate was added to 100 mL of hot methanol,After stirring and dissolving,filter,The filtrate was slowly evaporated to give a white solid, Yield 85percent.The molar ratio of (4- (aminomethyl) -2,3,5,6-tetramethylphenyl) methylamine and bis formylhydrazide is 1: 4 in the present invention;The reaction temperature was 150 ° C,Reaction time of 24 hours.Using "one pot"(4- (aminomethyl) -2,3,5,6-tetramethylphenyl) methylamine and bis formylhydrazide were prepared under heating to give 4- (4 - ((4H-1,2,4 Triazol-4-yl) methyl) -2,3,5,6-tetramethylphenyl) -4H-1,2,4-triazole (L).
85% at 150℃; for 24h; (4- (aminomethyl) -2,3,5,6-tetramethylphenyl) methylamine:The molar ratio of dibenzohydrazide is 1: 4 in the presence of a magnet,Reflux condenser and thermometer in a 50 mL three-necked round bottom flask(4- (aminomethyl) -2,3,5,6-tetramethylphenyl) methylamine (1 mmol)And dicarboxylic acid hydrazide (4 mmol)Start stirring at 150 oC,The reaction was carried out for 24 hours.After the reaction,The reaction solution was allowed to cool to room temperature,The resulting precipitate was added to 100 mL of warm methanol,After stirring and stirring, the filtrate was slowly evaporated to give a white solid,Yield 85percent.

 

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