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Chemical Structure| 3382-62-5 Chemical Structure| 3382-62-5

Structure of 3382-62-5

Chemical Structure| 3382-62-5

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Product Details of [ 3382-62-5 ]

CAS No. :3382-62-5
Formula : C13H10FNO
M.W : 215.22
SMILES Code : OC1=CC=CC=C1/C=N/C2=CC=C(F)C=C2
MDL No. :MFCD01111695

Safety of [ 3382-62-5 ]

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 [ 3382-62-5 ]

* 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 [ 3382-62-5 ]

[ 3382-62-5 ] Synthesis Path-Downstream   1~1

  • 1
  • europioum(III) chloride [ No CAS ]
  • [ 17217-57-1 ]
  • [ 3382-62-5 ]
  • C51H39EuF3N5O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
In methanol; at 60℃; for 5h;pH 6 - 7; General procedure: The synthesis of complexes was carried out by single potsynthesis. An anhydrous methanolic solution (10 mL) of 4-fluoro-N-salicylideneaniline (0.6456, 3 mmol) was addeddropwise to a vigorously stirred solution of 2,2?-bipyridine(0.1561, 1 mmol) in 10 mL methanol. To this solution ofligands, a methanolic solution of EuCl3 (0.2583 g, 1 mmol)was added slowly with continuous stirring. The pH of thereaction mixture obtained was adjusted to 6.0?7.0. Afteradjusting the pH, the reaction mixture was refluxed at 60 °C.The refluxing was continued for 5 h. The light yellow solutionso obtained was evaporated at room temperature to give thesolid compound which was extracted with diethyl ether. Thecompound obtained after extraction is C1 (Scheme 1).
 

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