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Chemical Structure| 144061-16-5 Chemical Structure| 144061-16-5

Structure of 144061-16-5

Chemical Structure| 144061-16-5

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Product Details of [ 144061-16-5 ]

CAS No. :144061-16-5
Formula : C11H6F3NO2S
M.W : 273.23
SMILES Code : O=C(C1=CSC(C2=CC=C(C(F)(F)F)C=C2)=N1)O
MDL No. :MFCD05865138

Safety of [ 144061-16-5 ]

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 [ 144061-16-5 ]

* 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 [ 144061-16-5 ]

[ 144061-16-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 175204-88-3 ]
  • [ 144061-16-5 ]
YieldReaction ConditionsOperation in experiment
With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; at 80℃; for 12h; General procedure: Toan oven-dried round bottom flask charged withethyl 2-(4-chlorophenyl)thiazole-4-carboxylate,55(176 mg, 0.62 mmol,1.0 equiv.) THF (6 mL) and MeOH (2mL) was added LiOH.H2O (78 mg, 1.86 mmol,3.0 equiv.).The reaction mixture was allowed to stir at 80 for 12 hr.The reaction mixture was cooled toroom temperatureand neutralized with 1N HCl. The resulting solution was extracted with ethyl acetate.The combined organic layer was dried overMgSO4,filtered,and concentrated under reduced pressureto give 2-(4-chlorophenyl) thiazole-4-carboxylic acid.
 

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