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CAS No. : | 108-26-9 | MDL No. : | MFCD00020699 |
Formula : | C4H6N2O | Boiling Point : | No data available |
Linear Structure Formula : | C3H3N2(CH3)(O) | InChI Key : | NHLAPJMCARJFOG-UHFFFAOYSA-N |
M.W : | 98.10 | Pubchem ID : | 7920 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With C33H30F6N4O3; In dichloromethane; at 20℃; for 24h;Inert atmosphere; | General procedure: To a solution of nitroolefin 3 (0.33 mmol) in CH2Cl2 (1.5 ml) was added bifunctional catalyst 1i (2 mg,0.0033 mmol, 1 mol %) and the mixture was stirred for 5 min under N2 atmosphere. Then pyrazolin-5-one 2 (0.4 mmol) was added to the mixture. Upon consumption of nitroolefin substrate (monitored by TLC), the reaction mixture was concentrated and purified by silica gel column chromatography to afford the conjugate addition products 4. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With acetic acid; In dimethyl sulfoxide; at 55℃; for 3h;Microwave irradiation; | General procedure: All reactions were carried out in PCR tubes at 50 μL scale. The reactantswere dissolved in DMSO to a final concentration of 40 mM (1.0equiv), and 0.3 μL glacial acetic acid (2.0 equiv) was added as a catalyst.The reaction mixtures were heated in a real-time PCR detection systems(Bio-Rad, CFX96) at 55 for 3 h,followed by cooing to roomtemperature. |
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