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Chemical Structure| 359647-66-8 Chemical Structure| 359647-66-8

Structure of 359647-66-8

Chemical Structure| 359647-66-8

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Product Details of [ 359647-66-8 ]

CAS No. :359647-66-8
Formula : C39H24N4
M.W : 548.63
SMILES Code : N(C1=CC=C(C#CC2=CC=NC=C2)C=C1)(C3=CC=C(C#CC4=CC=NC=C4)C=C3)C5=CC=C(C#CC6=CC=NC=C6)C=C5
MDL No. :MFCD34473405

Safety of [ 359647-66-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 359647-66-8 ]

* 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 [ 359647-66-8 ]

[ 359647-66-8 ] Synthesis Path-Downstream   1~4

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  • [ 19524-06-2 ]
  • [ 189178-09-4 ]
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  • [ 2510-22-7 ]
  • [ 4181-20-8 ]
  • [ 359647-66-8 ]
  • 3
  • [ 4181-20-8 ]
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  • 4
  • [ 15854-87-2 ]
  • [ 189178-09-4 ]
  • [ 359647-66-8 ]
YieldReaction ConditionsOperation in experiment
85% General procedure: The appropriate mono-, di- or tri-acetylene TPA derivative(200 mg) and 4-iodopyridine were dissolved in a mixture ofdioxane/piperidine (25 mL, 4/1). Ar was bubbled through themixture for 10 min and [Pd(PPh3)4] and CuI were added. The reactionmixture was stirred at 90 C for 12 h. The cooled reactionmixture was diluted with H2O (50 mL) and extracted with CH2Cl2(2 50 mL). The combined organic extracts were thenwashed withsaturated NH4Cl solution, brine, and dried. Finally, the solventswere evaporated under vacuum and the crude productwas purifiedby column chromatography (SiO2, appropriate eluent).
 

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