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Chemical Structure| 61636-28-0 Chemical Structure| 61636-28-0

Structure of 61636-28-0

Chemical Structure| 61636-28-0

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Product Details of [ 61636-28-0 ]

CAS No. :61636-28-0
Formula : C12H8N2O2S
M.W : 244.27
SMILES Code : O=C1C(C2=CSC(N)=N2)=CC3=C(O1)C=CC=C3
MDL No. :MFCD00481614

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Application In Synthesis of [ 61636-28-0 ]

* 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 [ 61636-28-0 ]

[ 61636-28-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 25365-71-3 ]
  • [ 61636-28-0 ]
  • (E)-3-{4-[({2-phenyl-1H-indol-3-yl}methylene)-amino]thiazol-2-yl}-2H-chromen-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With acetic acid; In ethanol; at 120℃; for 0.0833333h;Microwave irradiation; Green chemistry; General procedure: A mixture of 2,5-disubstituted-1H-indol-3-carboxaldehyde (1a-1d)(0.01 mol) with 3-(4-aminothiazol-2-yl)-2H-chromen-2-one (2a) or 3-(4-aminothiazol-2-yl)-6-bromo-2H-chromen-2-one (2e) (0.01 mol) in hot ethanol (5 mL) containing4-5 drops of glacial acetic acid was charged into an open borosil glass tube and MW irradiated for 4-5 minat 120C (Table 1). Upon completion of the process(TLC) the reaction mixture was cooled down to room temperature, washed with water and filtered off to get the corresponding pure compound [25].
 

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