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Chemical Structure| 17423-55-1 Chemical Structure| 17423-55-1

Structure of 17423-55-1

Chemical Structure| 17423-55-1

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Product Details of [ 17423-55-1 ]

CAS No. :17423-55-1
Formula : C14H14O2
M.W : 214.26
SMILES Code : COC1=CC=C(C2=CC=CC=C2)C=C1OC
MDL No. :N/A

Safety of [ 17423-55-1 ]

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 [ 17423-55-1 ]

* 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 [ 17423-55-1 ]

[ 17423-55-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5460-32-2 ]
  • [ 98-80-6 ]
  • [ 17423-55-1 ]
YieldReaction ConditionsOperation in experiment
93% With potassium carbonate; In ethanol; water; at 80℃; for 1h;Green chemistry;Catalytic behavior; General procedure: A mixture of aryl halide (1 mmol), phenylboronic acid(1.2 mmol), K2CO3 (2 mmol), Fe3O4-AuSF-SBA-15 nanocatalyst(50 mg or 0.64 mmol% of Au) and 5 mL of C2H5OH/H2O (1:1) wereadded to a 25 mL round-bottom flask and stirred at 80 C forappropriate times. After completion the reaction (controlled byTLC), the mixture was cooled and the catalyst was recovered by amagnet and washed three times with ethyl acetate and ethanol.The combined organic layer was dried over MgSO4. Then the solventwas evaporated and the residue was purified by column chromatographyand characterized by its 1H NMR, 13C NMR andmelting point.
 

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