ChemicalBook--->CAS DataBase List--->1481-02-3

1481-02-3

1481-02-3 Structure

1481-02-3 Structure
IdentificationMore
[Name]

1-METHYL-3-TRIFLUOROMETHYL-2-PYRAZOLIN-5-ONE
[CAS]

1481-02-3
[Synonyms]

1-METHYL-3-TRIFLUOROMETHYL-2-PYRAZOLIN-5-ONE
1-METHYL-3-(TRIFLUOROMETHYL)-4,5-DIHYDRO-1H-PYRAZOL-5-ONE
2-METHYL-5-(TRIFLUOROMETHYL)-2,4-DIHYDRO-3H-PYRAZOL-3-ONE
BUTTPARK 24\09-48
METHYL-3-TRIFLUOROMETHYL-2-PYRAZOLIN-5-ONE
1-Methyl-3-trifluormethyl-2-pyrazolin-5-one
1-Methyl-3-(trifluoromethyl)-2-pyrazolin-5-one 97%
1-Methyl-3-(trifluoromethyl)-2-pyrazolin-5-one97%
3-trifluoromethyl-1-methyl-1H-5-Pyrazolone
[EINECS(EC#)]

671-953-3
[Molecular Formula]

C5H5F3N2O
[MDL Number]

MFCD00051654
[Molecular Weight]

166.1
[MOL File]

1481-02-3.mol
Chemical PropertiesBack Directory
[Melting point ]

178 °C
[Boiling point ]

101.6±50.0 °C(Predicted)
[density ]

1.50±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

0.58±0.50(Predicted)
[Appearance]

White to off-white Solid
[BRN ]

5811070
[CAS DataBase Reference]

1481-02-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

25
[Safety Statements ]

45
[Hazard Note ]

Irritant
[HS Code ]

2933119000
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHYL-3-TRIFLUOROMETHYL-2-PYRAZOLIN-5-ONE(1481-02-3)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

1-methyl-3-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-5-one(1481-02-3)
[Alfa Aesar]

1-Methyl-3-trifluoromethyl-2-pyrazolin-5-one, 96%(1481-02-3)
Hazard InformationBack Directory
[Synthesis]

Ethyl 4,4,4-trifluoroacetoacetate

372-31-6

Methylhydrazine

60-34-4

1-METHYL-3-TRIFLUOROMETHYL-2-PYRAZOLIN-5-ONE

1481-02-3

0.1 mL of methylhydrazine and 10 mL of anhydrous ethanol were added to a 250 mL three-necked flask, stirred and heated to 50°C. Subsequently, 0.1 mol of ethyl trifluoroacetoacetate was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was heated to reflux for 5 hours. Upon completion of the reaction, the mixture was cooled to promote crystallization. The resulting yellow solid was collected by vacuum filtration and dried. The yield of the final product was 85.8%.

[References]

[1] Patent: CN103951663, 2016, B. Location in patent: Paragraph 0091; 0092; 0093
[2] Australian Journal of Chemistry, 2010, vol. 63, # 5, p. 785 - 791
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