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Chemical Structure| 5292-42-2 Chemical Structure| 5292-42-2

Structure of 5292-42-2

Chemical Structure| 5292-42-2

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Product Details of [ 5292-42-2 ]

CAS No. :5292-42-2
Formula : C8H4F4O2
M.W : 208.11
SMILES Code : O=C(OC)C1=CC(F)=C(F)C(F)=C1F
MDL No. :MFCD06203829
Boiling Point : No data available
InChI Key :MAEQYZYOSFAUAF-UHFFFAOYSA-N
Pubchem ID :600996

Safety of [ 5292-42-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 5292-42-2 ]

* 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 [ 5292-42-2 ]

[ 5292-42-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 827-08-7 ]
  • [ 616-38-6 ]
  • [ 5292-42-2 ]
  • 2
  • [ 1116-76-3 ]
  • [ 652-12-0 ]
  • [ 5292-42-2 ]
YieldReaction ConditionsOperation in experiment
92.3% In methanol; EXAMPLE 18 Into a 100 ml glass reactor equipped with a reflux condenser and a stirrer, 20 g (0.091 mol) of the tetrafluorophthalic anhydride prepared in Example 3 and 32.2 g (0.091 mol) of tri-n-octylamine were charged and 3.5 g (0.109 mol) of methanol was dropwise added thereto. Then, the mixture was reacted at 140 C. for 4 hours. After completion of the reaction, the reaction mixture was separated by distillation to obtain 17.5 g of 3,4,5,6-tetrafluorobenzoic acid methyl ester. The yield was 92.3%.
 

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