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[ CAS No. 35696-77-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 35696-77-6
Chemical Structure| 35696-77-6
Structure of 35696-77-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 35696-77-6 ]

CAS No. :35696-77-6 MDL No. :MFCD00041158
Formula : C9H12N2O2S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 212.27 Pubchem ID :-
Synonyms :

Safety of [ 35696-77-6 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P301+P310 UN#:2811
Hazard Statements:H301 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 35696-77-6 ]

* 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 [ 35696-77-6 ]

[ 35696-77-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 35696-77-6 ]
  • [ 17570-98-8 ]
  • N-(2,4-dimethoxyphenyl)-4-(2-pyridinyl)-1,3-thiazol-2-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
90% General procedure: 5.1.1 General procedure A (for synthesis of compounds 1-19). To 2-bromoacetylpyridine hydrobromide (1.0 equiv) in anhydrous ethanol (5 mL) was added the corresponding thiourea (1.0 equiv, 0.2 g) and the reaction mixture refluxed for 4 h. After cooling to ambient temperature the reaction mixture was poured into water. The pH of the mixture was adjusted to pH 8 with concentrated aqueous NH4OH and the mixture stirred for 2 h. The precipitate was filtered, washed with ethanol and dried to afford the title compound.
  • 2
  • [ 33904-03-9 ]
  • [ 35696-77-6 ]
YieldReaction ConditionsOperation in experiment
With ammonium hydroxide at 20℃;
  • 3
  • [ 35696-77-6 ]
  • [ 87080-27-1 ]
  • 1-(2,4-dimethoxyphenyl)-6-(4-hydroxy-2-methoxy-5-(2-methylbut-3-en-2-yl)phenyl)-4-(4-hydroxyphenyl)-5,6-dihydropyrimidin-2-thione [ No CAS ]
YieldReaction ConditionsOperation in experiment
43.11% With triethylamine; In N,N-dimethyl-formamide; toluene; at 100.0℃; for 6.0h; To the reactor was added 200 mg (1 mmol) of <strong>[87080-27-1]licorice chalcone A</strong> and 163.09 mg (1.3 mmol)1- (2,4-DimethylPhenyl)Thiourea,Add 50ml of toluene and 5mLDMF as the reaction solvent, add 0.5mL of triethylamine as a catalyst, heating sets of heatingTo 100 C, and the mixture was subjected to magnetic stirring for 6 hours. Thin layer chromatography to trace the reaction, after the end of the reaction, under reduced pressure, column chromatography, off the dry to obtain brown powder (135.70 mg), the total yield 43.11%
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