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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 5818-15-5 Chemical Structure| 5818-15-5

Structure of 5818-15-5

Chemical Structure| 5818-15-5

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Product Details of [ 5818-15-5 ]

CAS No. :5818-15-5
Formula : C3H8N2O
M.W : 88.11
SMILES Code : CCC(NN)=O
MDL No. :MFCD01333200
InChI Key :DXGIRFAFSFKYCF-UHFFFAOYSA-N
Pubchem ID :79890

Safety of [ 5818-15-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H315-H319-H335
Precautionary Statements:P261-P301+P310-P305+P351+P338
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 5818-15-5 ]

* 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 [ 5818-15-5 ]

[ 5818-15-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 14401-72-0 ]
  • [ 5818-15-5 ]
  • (E)-N'-(1-(3,5-dichlorophenyl)ethylidene)propionohydrazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
0.57 g With acetic acid; In ethanol; for 3h;Reflux; 0.50 g (2.64 mmol) of 1- (3,5-dichlorophenyl) ethan-1-one,A mixed solution of 0.28 g (3.17 mmol) of propionohydrazide, 5 ml of ethanol and 0.010 g of acetic acid was stirred under heating reflux for 3 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and the crystals precipitated in the reaction solution were collected by filtration to give 0.57 g of the objective compound as white crystals.
  • 2
  • [ 60159-37-7 ]
  • [ 5818-15-5 ]
  • (E)-N'-(1-(4-chloropyridin-2-yl)ethylidene)propionohydrazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
0.49 g With acetic acid; In ethanol; at 50 - 70℃; for 4h; 0.54 g (3.50 mmol) of 1- (4-chloropyridin-2-yl) ethan-1-one, 0.37 g (4.20 mmol) of propionohydrazide,3.6 ml of ethanol and 0.010 g of acetic acid was stirred at 50 C. for 3 hours and then stirred at 70 C. for 1 hour. After completion of the stirring, the reaction mixture was cooled to room temperature and then 20 ml of water was added. Subsequently, crystals precipitated in the reaction solution were collected by filtration to obtain 0.49 g of the objective compound as white crystals.
 

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