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[ CAS No. 1141757-83-6 ]

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Chemical Structure| 1141757-83-6
Chemical Structure| 1141757-83-6
Structure of 1141757-83-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1141757-83-6 ]

CAS No. :1141757-83-6 MDL No. :
Formula : C54H35N3 Boiling Point : -
Linear Structure Formula :- InChI Key :FXKMXDQBHDTQII-UHFFFAOYSA-N
M.W :725.88 Pubchem ID :68185634
Synonyms :

Safety of [ 1141757-83-6 ]

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

Application In Synthesis of [ 1141757-83-6 ]

* 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 [ 1141757-83-6 ]

[ 1141757-83-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1153-85-1 ]
  • [ 618442-57-2 ]
  • [ 1141757-83-6 ]
YieldReaction ConditionsOperation in experiment
82% (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) -9-phenylcarbazole,One equivalent (20 g, 40.49 mmol),3-Bromo-9-phenylcarbazole, 2Equivalent (26 g, 81 mmol), 33.5 g of K2CO3, 800 ml of toluene,And 200 ml of water was added to a 2-L 2-neck round bottom flask. The mixture was stirred at room temperature for 30 minutes,Pd (PPh3) 4 (1.4 g, 1.21 mmol) was added and refluxed for 24 hours.After the reaction was completed, the reaction mixture was extracted with methylene chloride, added with MgSO 4 and filtered.After removing the solvent of the obtained organic layer, it was purified by column chromatography to obtain intermediate compound 1 (24.80 g, yield 82%).
  • 2
  • [ 1126522-69-7 ]
  • [ 57103-20-5 ]
  • [ 1141757-83-6 ]
YieldReaction ConditionsOperation in experiment
60.9% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene; for 5h;Reflux; Inert atmosphere; Synthesis Example 1 Synthesis of H1-1 compound: 1.6 g of 3,6-dibromo-9-phenyl-9oxazole, 2.4 g of 9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9Eta-carbazole under a nitrogen atmosphere ,0.23 g of tetrakis(triphenylphosphine)palladium, 6 ml of 2M aqueous potassium carbonate solution,20 ml of toluene and 5 ml of ethanol were placed in a reaction vessel, and then heated and stirred at reflux temperature for 5 hours.After cooling to 40 C, the insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure to give a crude product.The crude product was purified by recrystallization (solvent: toluene/methanol) and dried.1.76 g (yield: 60.9%) of 3,6-bis(9'-phenyl-9Eta-carbazol-3-yl)-9-phenyl-9H-carbazole (Compound H1-1) is obtained as a brownish white powder.
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