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Chemical Structure| 126541-88-6 Chemical Structure| 126541-88-6

Structure of 126541-88-6

Chemical Structure| 126541-88-6

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Product Details of [ 126541-88-6 ]

CAS No. :126541-88-6
Formula : C9H7F3O3
M.W : 220.15
SMILES Code : O=C(OC)C1=CC=C(C(F)(F)F)C(O)=C1
MDL No. :MFCD18399431

Safety of [ 126541-88-6 ]

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 [ 126541-88-6 ]

* 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 [ 126541-88-6 ]

[ 126541-88-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 183170-69-6 ]
  • [ 126541-88-6 ]
  • tert-butyl 4-{1-[5-(methoxycarbonyl)-2-(trifluoromethyl)phenoxy]ethyl}piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With azodicarboxylic acid bis(2-methoxyethyl) ester; triphenylphosphine; In tetrahydrofuran; at 20℃; General procedure: Bis(2-methoxyethyl)azodicarboxylate (24 mg) was added to a solution of methyl 4'-hydroxy-6-(trifluoromethyl)[1,1'-biphenyl]-3-carboxylate (20 mg) obtained in Step 2, tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate (22 mg), and PPh3 (27 mg) in THF (0.7 mL), and the mixture was stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography to afford the title compound (20 mg).
 

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