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Chemical Structure| 78440-89-8 Chemical Structure| 78440-89-8

Structure of 78440-89-8

Chemical Structure| 78440-89-8

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Product Details of [ 78440-89-8 ]

CAS No. :78440-89-8
Formula : C7H7NO2
M.W : 137.14
SMILES Code : O=CC1=CC=C(C)NC1=O
MDL No. :MFCD07774136
Boiling Point : No data available
InChI Key :DGRLFJFWFJNPDX-UHFFFAOYSA-N
Pubchem ID :12722462

Safety of [ 78440-89-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 78440-89-8 ]

* 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 [ 78440-89-8 ]

[ 78440-89-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 78440-89-8 ]
  • [ 60481-51-8 ]
  • C15H17N3O [ No CAS ]
YieldReaction ConditionsOperation in experiment
In ethanol; at 20℃; for 2h; General procedure: The pyrazolo[4,3-c]pyridin-4-one derivatives were synthesizedby using compound 15 as starting material in two steps. Infirst step, the compound 15 (1 mmol, 137 mg) was dissolved inethanol (20 mL) and substituted phenylhydrazine hydrochloride(1.1 equivalent) was added. The reaction mixture was stirred atroom temperature for 2 h. The completion of reaction was monitoredby TLC. The resulted reaction mixture was allowed to cool toroom temperature. The solvent was evaporated under vacuum; ethanol (5 mL) was added and sonicated for 30 s to produce suspension.The resulted suspensions were kept in refrigerator for 1 hto settle down the suspended particles. The suspended particleswas filtered out and used for second step without further purification.In second step, the resulted solid was poured in boilingnitrobenzene at 210 C and stirred at same temperature for 15 min[27]. The completion of reaction was monitored by TLC. After thecompletion, the reaction mixture was allowed to cool to roomtemperature followed by silica gel column chromatography toisolate pure pyrazolo[4,3ec]pyridine4eone derivatives (12a-12p).
 

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