ChemicalBook--->CAS DataBase List--->33641-15-5

33641-15-5

33641-15-5 Structure

33641-15-5 Structure
IdentificationBack Directory
[Name]

5-Hydroxy-1-methylpyrazole
[CAS]

33641-15-5
[Synonyms]

Topramezon-001
2-methylpyrazol-3-ol
1-Methylpyrazol-5-ol
-Methyl-1H-pyrazol-5-ol
2-Methyl-2H-pyrazol-3-ol
1-methyl-1H-pyrazol-5-ol
1-methyl-5-hydroxypyrazol
1-Methyl-5-hydroxypyrazole
1H-Pyrazol-5-ol, 1-methyl-
5-Hydroxy-1-Methyl-5-pyrazole
1-Methyl-1H-pyrazol-3(2H)-one
1-Methyl-5-hydroxy-1H-pyrazole
5-HYDROXY-1-METHYL-1H-PYRAZOLE, 95%
REF DUPL: 5-Hydroxy-1-methyl-1H-pyrazole
[EINECS(EC#)]

213-317-6
[Molecular Formula]

C4H6N2O
[MDL Number]

MFCD05864418
[MOL File]

33641-15-5.mol
[Molecular Weight]

98.1032
Chemical PropertiesBack Directory
[Melting point ]

110-114 °C
[Boiling point ]

217.7±13.0 °C(Predicted)
[density ]

1.22±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

soluble in DMSO, Methanol
[form ]

powder to crystal
[pka]

9.07±0.23(Predicted)
[color ]

White to Orange to Green
[InChI]

InChI=1S/C4H6N2O/c1-6-4(7)2-3-5-6/h2-3,7H,1H3
[InChIKey]

CMXOTACIOGGSNH-UHFFFAOYSA-N
[SMILES]

N1(C)C(O)=CC=N1
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H318-H335
[Precautionary statements ]

P280-P301+P312+P330-P302+P352-P305+P351+P338+P310
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933199090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

5-Hydroxy-1-methylpyrazole is a pyrazole derivative used as an intermediate in the preparation of herbicides.
[Synthesis]

1H-Pyrazole-4-carboxylic acid, 1-methyl-, ethyl ester

88398-78-1

5-Hydroxy-1-methylpyrazole

33641-15-5

The general procedure for the synthesis of 1-methyl-5-hydroxypyrazole-4-carboxylic acid from ethyl 1-methyl-5-hydroxypyrazole-4-carboxylate is as follows: 22 g of sodium hydroxide was dissolved in 300 mL of water, 42.5 g of intermediate (ethyl 1-methyl-5-hydroxypyrazole-4-carboxylate) was added, and the reaction was stirred for 3 hr at 40 °C, then cooled to room temperature. 55 mL of concentrated hydrochloric acid was added dropwise, followed by heating and refluxing for 3 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, 200 mL of anhydrous ethanol was added to the residue, and the precipitate was collected by filtration after thorough stirring. The filtrate was concentrated under reduced pressure to give 24 g of white solid product (1-methyl-5-hydroxypyrazole) in 98.0% yield and 96.50% HPLC purity.

[References]

[1] Patent: CN105218449, 2016, A. Location in patent: Paragraph 0063; 006=5
Spectrum DetailBack Directory
[Spectrum Detail]

5-Hydroxy-1-methylpyrazole(33641-15-5)1HNMR
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