3-Methyl-3-pyrazolin-5-one

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3-Methyl-3-pyrazolin-5-one manufacturers

3-Methyl-3-pyrazolin-5-one Basic information
Product Name:3-Methyl-3-pyrazolin-5-one
Synonyms:AKOS B028792;3-METHYL-3-PYRAZOLIN-5-ONE;3 METHYLPYRAZOLONE;3-METHYL-3-PARAZOLIN-5-ONE;3-METHYL-2-PYRAZOLIN-5-ONE (PILOT);1,2-Dihydro-3-methyl-5H-pyrazol-5-one;3-Hydroxy-5-methyl-1H-pyrazole;3-Methyl-3-pyrazoline-5-one
CAS:4344-87-0
MF:C4H6N2O
MW:98.1
EINECS:
Product Categories:Building Blocks;C3 to C5;Chemical Synthesis;Heterocyclic Building Blocks;Building Blocks;Heterocyclic Building Blocks;Pyrazoles;Heterocyclic Compounds
Mol File:4344-87-0.mol
3-Methyl-3-pyrazolin-5-one Structure
3-Methyl-3-pyrazolin-5-one Chemical Properties
Melting point 223-225 °C (lit.)
density 1.107±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility 1 M NH4OH: soluble25mg/mL, clear, colorless (in methanol)
form solid
pka9.04±0.70(Predicted)
color Off White
InChI1S/C4H6N2O/c1-3-2-4(7)6-5-3/h2H,1H3,(H2,5,6,7)
InChIKeyWGVHNCAJPFIFCR-UHFFFAOYSA-N
SMILESCC1=CC(=O)NN1
CAS DataBase Reference4344-87-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-36
WGK Germany 3
HS Code 2933119000
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
3-Methyl-3-pyrazolin-5-one Usage And Synthesis
Chemical PropertiesLight yellow crystalline powder
Uses3-Methyl-3-pyrazolin-5-one was used in the preparation of substituted 4-alkyl(cycloalkyl)-2-amino-3-cyano-4H-pyrans.
General Description3-Methyl-3-pyrazolin-5-one is an intermediate in the synthesis of heterocyclic compounds. Crystal structure of 3-methyl-3-pyrazolin-5-one was studied.
Synthesis
Ethyl acetoacetate

141-97-9

3-Methyl-3-pyrazolin-5-one

4344-87-0

GENERAL METHODS: Phenylhydrazine (1 mmol), ethyl acetoacetate (1 mmol) and cobalt doped ZnS nanoparticles (5 mol%) were mixed in a Borosil beaker. The reaction mixture was homogeneously mixed using a glass rod and placed in an infrared reactor (360 W) for irradiation. The reaction process was monitored by thin layer chromatography (TLC). After completion of the reaction, the mixture was cooled to room temperature. Subsequently, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent to give the crude product. The crude product was purified by recrystallization from hot ethanol. Nanoparticles were recovered by sonication of the aqueous phase and could be reused four times in the same reaction.

References[1] Journal of Molecular Catalysis A: Chemical, 2013, vol. 373, p. 61 - 71
[2] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2016, vol. 55B, # 4, p. 507 - 516
[3] Patent: WO2015/200650, 2015, A1. Location in patent: Paragraph 0532-0534
[4] Chemische Berichte, 1896, vol. 29, p. 257
[5] Journal fuer Praktische Chemie (Leipzig), 1889, vol. <2> 39, p. 52
3-Methyl-3-pyrazolin-5-one Preparation Products And Raw materials
Raw materialsEthyl acetoacetate-->HYDRAZINE
Preparation Products3-Methyl-1H-pyrazole-4-carbaldehyde-->Methyl 2-butynoate-->3-Hydroxy-5-Methyl-pyrazole-1-carboxylic acid tert-butyl ester
Tag:3-Methyl-3-pyrazolin-5-one(4344-87-0) Related Product Information
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