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Chemical Structure| 103788-60-9 Chemical Structure| 103788-60-9

Structure of 103788-60-9

Chemical Structure| 103788-60-9

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Product Details of [ 103788-60-9 ]

CAS No. :103788-60-9
Formula : C10H7NO3S
M.W : 221.23
SMILES Code : O=C(NC/1=O)SC1=C\C2=CC=C(O)C=C2
MDL No. :MFCD00640639

Safety of [ 103788-60-9 ]

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 [ 103788-60-9 ]

* 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 [ 103788-60-9 ]

[ 103788-60-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 103788-60-9 ]
  • [ 129722-34-5 ]
  • 5-[[p-[4-(2-oxo-3,4-dihydro-1H-quinol-7-yloxy)butoxy]phenyl]methylidene]-1,3-thiazolidine-2,4-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
58% General procedure: To 0.23 g of the compounds 23a-23c (1.0 mmol) in 5 cm3dimethylformamide 0.29 g potassium carbonate(2.0 mmol) was added and the reaction mass was stirred for1 h at 50 C. To the stirred reaction mixture, 0.30 gcompound 22 (1.0 mmol) and 166 mg potassium iodide(1.0 mmol) were added and reaction mixture were furtherstirred at 50 C for 16 h. After completion of reaction, themass was cooled at room temperature. Then water wasadded and the precipitated product was filtered to obtainthe crude product. This was re-crystallized from ethylacetate to get the pure compounds 24a-24c.
  • 2
  • [ 103788-60-9 ]
  • [ 17329-87-2 ]
  • C18H13N3O6S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 24h; General procedure: Final products 3k-3y were synthesized by condensing 2k-2y with compound 1 in equimolar ratio in the presence of base such as potassium carbonate in Dimethylformamide. The reaction was allowed to stir at room temperature for 24 hrs, the water was added to generate the crude products, which was filtered and further purified by recrystallization or TLC column chromatography.
 

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