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Chemical Structure| 92967-67-4 Chemical Structure| 92967-67-4

Structure of 92967-67-4

Chemical Structure| 92967-67-4

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Product Details of [ 92967-67-4 ]

CAS No. :92967-67-4
Formula : C16H8N2O2
M.W : 260.25
SMILES Code : O=C(C1=CC=C(C#N)C=C1)C(C2=CC=C(C#N)C=C2)=O
MDL No. :MFCD32632581

Safety of [ 92967-67-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 92967-67-4 ]

* 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 [ 92967-67-4 ]

[ 92967-67-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 92967-67-4 ]
  • [ 4506-66-5 ]
  • C38H18N8 [ No CAS ]
YieldReaction ConditionsOperation in experiment
25% With sodium acetate; In butan-1-ol; at 120℃; for 20h; 10037] 1 ,2,4,5-l3enzenetetramine tetrahydrochloride (0.5 g, 1.76 mmol, and commercially available from Alfa Aesar) and the product in Formula 17 (1 g, 3.85 mmol) were put into a reaction bottle. Sodium acetate (0.576 g, 7.02 mmol) and n-butanol (50 mE) were added into the bottle. The mixture in the bottle was heated to 120 C. to react for 20 hours. A yellow precipitate was formed in a solution of the reaction result, and the yellow precipitate was then collected by filtering. The filtered cake was washed by n-hexane and ethyl ether, and then purified by thermal sublimation to obtain 0.8 g of a bright yellow powder (yield=25%). The above reaction is shown in Formula 18. The spectra of the product in Formula 18 are listed below: ?H NMR (400 MHz, CDC13): oe 9.08(s, 2H), 7.72(s, 16H). HRMS (El, mlz): cald. for C38H18N8: 586.1654, Found: 586.1649(M+).
25% With sodium acetate; In butan-1-ol; at 120℃; for 20h; The purchased Alfa Aesar 1, 2, 4, 5 - benzene tetramine four hydrochloride (0.5g, 1 . 76mmol) monomeric 17 product (1g, 3.85mmol) into the reaction bottle, add sodium acetate (0.576g, 7 . 02mmol) and butanol (50 ml), heated to 120 C reaction 20 hours. After the reaction, at this moment the solution yellow precipitate, then the sediment filtration and separation, and the normal hexane and ethyl ether washing the yellow solid, then the yellow solid via the heat sublimation purification is obtained when the bright yellow powder 0.8g, yield 25%.
 

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