ChemicalBook--->CAS DataBase List--->26308-42-9

26308-42-9

26308-42-9 Structure

26308-42-9 Structure
IdentificationBack Directory
[Name]

3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID
[CAS]

26308-42-9
[Synonyms]

AKOS PAO-0874
CHEMBRDG-BB 4402465
TIMTEC-BB SBB010349
ASINEX-REAG BAS 07751205
3-ETHYL-1-METHYLPYRAZOLE-5-CARBOXYLIC ACID
5-ethyl-2-methyl-3-pyrazolecarboxylic acid
5-ethyl-2-methylpyrazole-3-carboxylic acid
5-ethyl-2-methyl-pyrazole-3-carboxylic acid
3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID
5-ETHYL-2-METHYL-2H-PYRAZOLE-3-CARBOXYLIC ACID
1H-Pyrazole-5-carboxylic acid, 3-ethyl-1-Methyl-
3-ethyl-1-methyl-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)
[Molecular Formula]

C7H10N2O2
[MDL Number]

MFCD03086079
[MOL File]

26308-42-9.mol
[Molecular Weight]

154.17
Chemical PropertiesBack Directory
[Boiling point ]

320.8±30.0 °C(Predicted)
[density ]

1.23±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

3.11±0.25(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H302-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID(26308-42-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID ETHYL ESTER

128537-26-8

3-ETHYL-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID

26308-42-9

General procedure for the synthesis of 3-ethyl-1-methyl-1H-pyrazole-5-carboxylic acid from ethyl 3-ethyl-1-methyl-1H-pyrazole-5-carboxylate: ethyl 3-ethyl-1-methyl-1H-pyrazole-5-carboxylate (50 mmol), sodium hydroxide (150 mmol), water (120 mL), and ethanol (20 mL) were mixed, and the reaction was stirred under reflux conditions for 4-5 hours. After completion of the reaction, the reaction solution was cooled to room temperature and separated by extraction with ethyl acetate. The aqueous phase was collected and the pH was adjusted to 5-6 with dilute hydrochloric acid, acidified and left to precipitate the product. The precipitate was collected by filtration and dried to give 3-ethyl-1-methyl-1H-pyrazole-5-carboxylic acid in 4.8 g yield.

[References]

[1] Journal of Agricultural and Food Chemistry, 2012, vol. 60, # 6, p. 1470 - 1479
[2] Patent: CN106608873, 2017, A. Location in patent: Paragraph 0111; 0112; 0115
[3] Patent: CN106608872, 2017, A. Location in patent: Paragraph 0104; 0107
[4] Chemical Papers, 2017, vol. 71, # 11, p. 2053 - 2061
[5] European Journal of Medicinal Chemistry, 2018, vol. 149, p. 170 - 181
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