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Chemical Structure| 75919-92-5 Chemical Structure| 75919-92-5

Structure of 75919-92-5

Chemical Structure| 75919-92-5

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Product Details of [ 75919-92-5 ]

CAS No. :75919-92-5
Formula : C14H11NO4
M.W : 257.24
SMILES Code : CC(C1=CC=C(OC2=CC=C([N+]([O-])=O)C=C2)C=C1)=O
MDL No. :MFCD00052956

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Application In Synthesis of [ 75919-92-5 ]

* 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 [ 75919-92-5 ]

[ 75919-92-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 284462-56-2 ]
  • [ 32315-10-9 ]
  • [ 5369-19-7 ]
  • [ 350-46-9 ]
  • [ 99-93-4 ]
  • [ 75919-92-5 ]
YieldReaction ConditionsOperation in experiment
Syntheses of Exemplified Compounds (see Tables for Compound Characterization) Entry 1: 4-(3-N-Methylcarbamoylphenoxy)aniline was prepared according to Method A13. According to Method C3, <strong>[5369-19-7]3-tert-butylaniline</strong> was reacted with bis(trichloromethyl)carbonate followed by 4-(3-N-Methylcarbamoylphenoxy)aniline to afford the urea. Entry 2: 4-Fluoro-1-nitrobenzene and p-hydroxyacetophenone were reacted according to Method A13, Step 1 to afford the 4-(4-acetylphenoxy)-1-nitrobenzene.
Syntheses of Exemplified Compounds (See Tables for Compound Characterization) Entry 1: 4-(3-N-Methylcarbamoylphenoxy)aniline was prepared according to Method A13. According to Method C3, <strong>[5369-19-7]3-tert-butylaniline</strong> was reacted with bis(trichloromethyl)carbonate followed by 4-(3-N-Methylcarbamoylphenoxy)aniline to afford the urea. Entry 2: 4-Fluoro-1-nitrobenzene and p-hydroxyacetophenone were reacted according to Method A13, Step 1 to afford the 4-(4-acetylphenoxy)-1-nitrobenzene.
SYNTHESES OF EXEMPLIFIED COMPOUNDS (See Tables for Compound Characterization) Entry 1: 4-(3-N-Methylcarbamoylphenoxy)aniline was prepared according to Method A13. According to Method C3, <strong>[5369-19-7]3-tert-butylaniline</strong> was reacted with bis(trichloromethyl)carbonate followed by 4-(3-N-Methylcarbamoylphenoxy)aniline to afford the urea. Entry 2: 4-Fluoro-1-nitrobenzene and p-hydroxyacetophenone were reacted according to Method A13, Step 1 to afford the 4-(4-acetylphenoxy)-1-nitrobenzene.
 

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