| Identification | Back Directory | [Name]
ETHYL 1-METHYL-3-PHENYL-1H-PYRAZOLE-5-CARBOXYLATE | [CAS]
10250-63-2 | [Synonyms]
SALOR-INT L201367-1EA 1H-Pyrazole-5-carboxylic acid, 1 Ethyl 1-Methyl-3-phenylpyrazole-5-carboxylate ETHYL 1-METHYL-3-PHENYL-1H-PYRAZOLE-5-CARBOXYLATE Ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate 97% 1H-Pyrazole-5-carboxylic acid, 1-methyl-3-phenyl-, ethyl ester JR-13855, Ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate, 95% 5-(Ethoxycarbonyl)-1-methyl-3-phenyl-1H-pyrazole, 1-[5-(Ethoxycarbonyl)-1-methyl-1H-pyrazol-3-yl]benzene | [Molecular Formula]
C13H14N2O2 | [MDL Number]
MFCD03933288 | [MOL File]
10250-63-2.mol | [Molecular Weight]
230.26 |
| Chemical Properties | Back Directory | [Melting point ]
27 °C | [Boiling point ]
380.6±30.0 °C(Predicted) | [density ]
1.13±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
0.04±0.10(Predicted) |
| Hazard Information | Back Directory | [Synthesis]
To a solution of ethyl 2,4-dioxo-4-phenylbutyrate (1.0 g, 4.5 mmol), methylhydrazine sulfate (1.0 g, 6.8 mmol) and sodium hydroxide (0.5 g, 13.6 mmol) in ethanol (50 mL) was added the reaction mixture. The reaction mixture was stirred at 70 °C overnight. After completion of the reaction, the reaction was quenched with ice water (100 mL), extracted with ethyl acetate, the organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to give the crude product. The crude product was purified by silica gel column chromatography eluting with appropriate eluent to give ethyl 1-methyl-3-phenyl-1H-pyrazole-5-carboxylate (247.5 mg, 23.9%). Mass spectrum (ESI) m/z: 231.1 [M + 1]. | [References]
[1] Patent: US2018/271846, 2018, A1. Location in patent: Paragraph 0176; 0178; 0179 |
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