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Chemical Structure| 64267-19-2 Chemical Structure| 64267-19-2

Structure of 64267-19-2

Chemical Structure| 64267-19-2

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Product Details of [ 64267-19-2 ]

CAS No. :64267-19-2
Formula : C12H10O4
M.W : 218.21
SMILES Code : O=C1C(C(C)=O)=CC2=C(O1)C=C(OC)C=C2
MDL No. :MFCD01241792

Safety of [ 64267-19-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 64267-19-2 ]

* 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 [ 64267-19-2 ]

[ 64267-19-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 50-00-0 ]
  • [ 64267-19-2 ]
  • [ 25150-61-2 ]
  • 7-methoxy-3-(3-(pyrrolidin-1-yl)propanoyl)-2H-chromen-2-one hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
50.5% The amine is selected from tetrahydropyrrole, and the amount and ratio of the operation and the raw material reagent are the same as above. After refluxing for 11 hours, it is cooled to room temperature, and a solid precipitates.Filtration and washing with a small amount of acetone and ethanol gave a pale yellow solid (0.34 g). Yield: 50.5%. 1.7 g (20 mmol) of piperidine and 0.6 g (20 mmol) of paraformaldehyde were added to 25 mL of ethanol, and then the pH of the solution was adjusted to 2 to 3 with concentrated hydrochloric acid.After heating under reflux, 0.44 g (2 mmol) of 3-acetyl-7-ethoxycoumarin obtained in Preparation Example 3 was added, and reflux was continued for 12 hours.After cooling to room temperature, it was filtered and washed with a small amount of acetone to give a white solid (0.3 g). Yield: 45%.
 

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