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Chemical Structure| 54001-10-4 Chemical Structure| 54001-10-4

Structure of 54001-10-4

Chemical Structure| 54001-10-4

Ethyl 4-Methyl-2-(3-methylphenyl)thiazole-5-carboxylate

CAS No.: 54001-10-4

4.5 *For Research Use Only !

Cat. No.: A287984 Purity: 95+%

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Product Details of [ 54001-10-4 ]

CAS No. :54001-10-4
Formula : C14H15NO2S
M.W : 261.34
SMILES Code : O=C(C1=C(C)N=C(C2=CC=CC(C)=C2)S1)OCC
MDL No. :MFCD11845862

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Application In Synthesis of [ 54001-10-4 ]

* 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 [ 54001-10-4 ]

[ 54001-10-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2362-63-2 ]
  • [ 609-15-4 ]
  • [ 54001-10-4 ]
YieldReaction ConditionsOperation in experiment
72% In ethanol; at 0℃; for 16h;Reflux; General procedure: A solution of 24a-f (1 equiv) and ethyl 2-chloroacetoacetate (1.2 equiv) in ethanol (25mL) was heated to reflux for 6h, then the mixture was allowed to stand at 0C for 10h, and a white needle crystal was precipitate out. The reaction mixture was filtered and the filter cake was washed with 10mL of ethanol, dried in vacuum to give the desired product.
68% In ethanol; for 6h;Reflux; General procedure: A solution of 5a-h (1 equiv) and ethyl 2-chloroacetoacetate (1.2 equiv) in ethanol (25mL) was heated to reflux for 6h, then the mixture was allowed to stand at 0C for 10h, and a white needle crystal was precipitate out. The reaction mixture was filtered and the filter cake was washed with ethanol (10mL), dried to give the title compounds.
  • 2
  • [ 2362-63-2 ]
  • [ 638-07-3 ]
  • [ 54001-10-4 ]
YieldReaction ConditionsOperation in experiment
71% In ethanol; for 6h;Reflux; General procedure: To a solution of benzamide 11a-u (1 equiv) in THF (30mL) was added Lawesson’s reagent (0.6 equiv), and the mixture was heated to reflux for 4 hrs. The reaction mixture was concentrated invacuo,then diluted with ethyl acetate (30 ml), and washed with 1N NaHCO3 (3× 20 mL) and brine (2 × 20 mL). The organic layer was dried over anhydrous sodium sulfate,filtered and evaporated under reduced pressure. The crude product was purified by silica gel column chromatography using a mixture of dichloromethane/methanol(100:1, v/v) as eluent to afford a yellow solid product.A solution of the obtained solid 12a-u (1 equiv) and ethyl 2-chloroacetoacetate (1.2 equiv) in ethanol (25 ml) was heated to reflux for 6 h, then the mixture was allowed to stand at 0 C for 10 hrs, and a white needle crystal was precipitate out.The reaction mixture was filtered and the filter cake was washed with 10 mL of ethanol, dried in vacuum to give the desired product.
 

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