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Chemical Structure| 5292-53-5 Chemical Structure| 5292-53-5

Structure of 5292-53-5

Chemical Structure| 5292-53-5

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Product Details of [ 5292-53-5 ]

CAS No. :5292-53-5
Formula : C14H16O4
M.W : 248.27
SMILES Code : O=C(OCC)/C(C(OCC)=O)=C/C1=CC=CC=C1
MDL No. :MFCD00009149
InChI Key :VUWPIBNKJSEYIN-UHFFFAOYSA-N
Pubchem ID :94751

Safety of [ 5292-53-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H319-H332
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 5292-53-5 ]

* 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 [ 5292-53-5 ]

[ 5292-53-5 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 5292-53-5 ]
  • [ 1198-97-6 ]
  • 2
  • [ 5292-53-5 ]
  • [ 446065-11-8 ]
  • diethyl 2-(cyclohexyl(phenyl)methyl)malonate [ No CAS ]
  • 3
  • [ 172512-93-5 ]
  • [ 5292-53-5 ]
  • C23H23NO4 [ No CAS ]
  • C23H23NO4 [ No CAS ]
  • 4
  • [ 2725-60-2 ]
  • [ 5292-53-5 ]
  • [ 6963-62-8 ]
  • C22H24N2O6S [ No CAS ]
YieldReaction ConditionsOperation in experiment
35% With ethanol; sodium ethanolate; for 1.0h; General procedure: To a stirred solution of arylidenemalonate 4 (0.5 mmol) and a -diazo- b -ketosulfone 2 (143 mg, 0.6 mmol, 1.2 equiv) in dry EtOH(5 mL) was added Cs2CO3 (245 mg, 0.75 mmol, 1.5 equiv) at 0C andthe resulting mixture was stirred until the reaction was complete(monitored by TLC). Then the reaction mixture was concentrated invacuo and the crude residue was directly subjected to silica gel column chromatography (pet ether/ethyl acetate: 8/2) to affordpure pyrazole carboxylate 5.
18% With ethanol; sodium ethanolate; for 5.0h; General procedure: To a stirred solution of arylidenemalonate 4 (0.5 mmol) and a -diazo- b -ketosulfone 2 (143 mg, 0.6 mmol, 1.2 equiv) in dry EtOH(5 mL) was added Cs2CO3 (245 mg, 0.75 mmol, 1.5 equiv) at 0C andthe resulting mixture was stirred until the reaction was complete(monitored by TLC). Then the reaction mixture was concentrated invacuo and the crude residue was directly subjected to silica gel column chromatography (pet ether/ethyl acetate: 8/2) to affordpure pyrazole carboxylate 5.
  • 5
  • [ 2725-60-2 ]
  • [ 5292-53-5 ]
  • [ 6963-62-8 ]
YieldReaction ConditionsOperation in experiment
70% With ethanol; caesium carbonate; for 4.0h; General procedure: To a stirred solution of arylidenemalonate 4 (0.5 mmol) and a -diazo- b -ketosulfone 2 (143 mg, 0.6 mmol, 1.2 equiv) in dry EtOH(5 mL) was added Cs2CO3 (245 mg, 0.75 mmol, 1.5 equiv) at 0C andthe resulting mixture was stirred until the reaction was complete(monitored by TLC). Then the reaction mixture was concentrated invacuo and the crude residue was directly subjected to silica gel column chromatography (pet ether/ethyl acetate: 8/2) to affordpure pyrazole carboxylate 5.
  • 6
  • [ 5292-53-5 ]
  • [ 6963-62-8 ]
YieldReaction ConditionsOperation in experiment
96% With ethanol; caesium carbonate; at 80.0℃; for 0.25h;Microwave irradiation; General procedure: In a 10mL microwave glass vial containing EtOH (1mL), was added pyrazoline 6 (0.1mmol) followed by Cs2CO3 (16.5mg, 0.05mmol, 0.5 equiv) and the resulting mixture was subjected to microwave irradiation for 10-15minat 80C until the completion of reaction (monitored by TLC). After removal of EtOH in vacuo, the residue was treated with water (10mL) and the aqueous layer was extracted with EtOAc (2×10mL). The combined organic layer was dried over anhydrous Na2SO4, filtered and the filtrate was then concentrated in vacuo. The residue was recrystallized from EtOAc/hexane (1:1) to obtain pure 5 in quantitative yields.
 

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