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Chemical Structure| 1295583-21-9 Chemical Structure| 1295583-21-9

Structure of 1295583-21-9

Chemical Structure| 1295583-21-9

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Product Details of [ 1295583-21-9 ]

CAS No. :1295583-21-9
Formula : C8H10N2O2
M.W : 166.18
SMILES Code : O=C(OC)/C=C/C1=CN(C)N=C1
MDL No. :MFCD23713913
InChI Key :RFUOSGKQKNFRGH-ONEGZZNKSA-N
Pubchem ID :21936263

Safety of [ 1295583-21-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P210-P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501

Application In Synthesis of [ 1295583-21-9 ]

* 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 [ 1295583-21-9 ]

[ 1295583-21-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5927-18-4 ]
  • [ 35344-95-7 ]
  • [ 1295583-21-9 ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In 1,4-dioxane; dimethyl sulfoxide; at 20 - 100℃; (E)-methyl 3-(l -methyl- lH-pyrazol-4-yl)acrylateCs2C03 (1.304g, 4 mmol) was added to a solution of lH-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> (0.192 g, 2 mmol) in dioxane (8 mL) at room temperature. Trimethylphosphonoacetate (0.364g, 0.40 mmol) was added to this suspension, followed by DMSO (2 mL). The reaction mixture was heated to 100°C overnight. It was then diluted with EtOAc (40 mL), and washed with water (40 mL) and brine (20 mL). The organic layer was concentrated under vacuum. The crude was purified by silica gel column chromatography using a 0-100percent gradient of EtOAc in hexanes to provide (E)-methyl 3 -(1 -methyl- lH-pyrazol-4- yl)acrylate (0.278 g). ES+ (M+H)+ 167
0.278 g With caesium carbonate; In 1,4-dioxane; dimethyl sulfoxide; at 20 - 100℃; Cs2CO3 (1.304 g, 4 mmol) was added to a solution of <strong>[35344-95-7]1H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong></strong> (0.192 g, 2 mmol) in dioxane (8 mL) at room temperature. Trimethylphosphonoacetate (0.364 g, 0.40 mmol) was added to this suspension, followed by DMSO (2 mL). The reaction mixture was heated to 100° C. overnight. It was then diluted with EtOAc (40 mL), and washed with water (40 mL) and brine (20 mL). The organic layer was concentrated under vacuum. The crude was purified by silica gel column chromatography using a 0-100percent gradient of EtOAc in hexanes to provide (E)-methyl 3-(1-methyl-1H-pyrazol-4-yl)acrylate (0.278 g). ES+(M+H)+167
 

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