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Chemical Structure| 98953-13-0 Chemical Structure| 98953-13-0

Structure of 98953-13-0

Chemical Structure| 98953-13-0

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Product Details of [ 98953-13-0 ]

CAS No. :98953-13-0
Formula : C9H10N2O3
M.W : 194.19
SMILES Code : O=C(C1=CC=C(OCCO2)C2=C1)NN
MDL No. :MFCD01536451

Safety of [ 98953-13-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 98953-13-0 ]

* 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 [ 98953-13-0 ]

[ 98953-13-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 18944-77-9 ]
  • [ 98953-13-0 ]
  • [ 1432346-50-3 ]
YieldReaction ConditionsOperation in experiment
60% With trichlorophosphate; at 110℃; for 5h; General procedure: An equimolar compound 6 (0.001 mol) and substituted cinnamic acid in phosphoryl chloride was refluxed for 5 h, Then reaction mixture was cooled, poured into ice-coldwater and neutralized with 20% NaHCO3 solution. The resultant solid was filtered, washed with water and recrystallized from ethanol to give the title compounds.
  • 2
  • [ 939-57-1 ]
  • [ 98953-13-0 ]
  • [ 1432346-73-0 ]
YieldReaction ConditionsOperation in experiment
77% With trichlorophosphate; at 110℃; for 5h; General procedure: An equimolar compound 6 (0.001 mol) and substituted cinnamic acid in phosphoryl chloride was refluxed for 5 h, Then reaction mixture was cooled, poured into ice-coldwater and neutralized with 20% NaHCO3 solution. The resultant solid was filtered, washed with water and recrystallized from ethanol to give the title compounds.
  • 3
  • [ 18944-77-9 ]
  • [ 98953-13-0 ]
  • [ 1615677-99-0 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20℃; for 8h; General procedure: An equimolar compound 6 (0.001mol) and substituted cinnamic acid in anhydrous CH2Cl2 was stirred for 8h with carbodiimide hydrochloride (0.0015mmol) and N-hydroxybenzotriazole (0.0005mmol). Then reaction mixture was extracted twice using ethyl acetate and water. The organic layer was evaporated and recrystallized from ethanol to give the title compounds.
  • 4
  • [ 939-57-1 ]
  • [ 98953-13-0 ]
  • [ 1615678-02-8 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20℃; for 8h; General procedure: An equimolar compound 6 (0.001mol) and substituted cinnamic acid in anhydrous CH2Cl2 was stirred for 8h with carbodiimide hydrochloride (0.0015mmol) and N-hydroxybenzotriazole (0.0005mmol). Then reaction mixture was extracted twice using ethyl acetate and water. The organic layer was evaporated and recrystallized from ethanol to give the title compounds.
 

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