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Chemical Structure| 15789-03-4 Chemical Structure| 15789-03-4

Structure of 15789-03-4

Chemical Structure| 15789-03-4

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Product Details of [ 15789-03-4 ]

CAS No. :15789-03-4
Formula : C9H11NO2
M.W : 165.19
SMILES Code : O=C(N(C)C)C1=CC=CC(O)=C1
MDL No. :MFCD01168918
InChI Key :TULKODADVOEVTR-UHFFFAOYSA-N
Pubchem ID :637524

Safety of [ 15789-03-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 15789-03-4 ]

* 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 [ 15789-03-4 ]

[ 15789-03-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 72802-25-6 ]
  • [ 15789-03-4 ]
  • 3-(5-acetyl-2-nitrophenoxy)-N,N-dimethylbenzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
1.8 g With potassium carbonate; In N,N-dimethyl-formamide; at 100℃; for 2h;Inert atmosphere; (2) Dissolve 3-hydroxy-N, N-dimethylbenzamide (2g) and <strong>[72802-25-6]3-fluoro-4-nitroacetophenone</strong> (3g) in anhydrous DMF (20mL), add under nitrogen protection Anhydrous potassium carbonate powder (3g);The reaction was performed at 100 C for 2 hours, cooled to room temperature, extracted with dichloromethane, the organic phase was dried, concentrated, and methyl tert-butyl ether was crystallized to obtain compound 3-(5-acetyl-2-nitrophenoxy)-N,N-dimethylbenzamide(1.8 g, white solid);
 

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