ChemicalBook--->CAS DataBase List--->5932-27-4

5932-27-4

5932-27-4 Structure

5932-27-4 Structure
IdentificationBack Directory
[Name]

Ethyl pyrazole-3-carboxylate
[CAS]

5932-27-4
[Synonyms]

3-Carbethoxypyrazole
3-(Ethoxycarbonyl)pyrazole
Ethyl 3-Pyrazolecarboxylate
Ethyl pyrazole-5-carboxylate
Ethyl pyrazole-3-carboxylate
Eythyl 3-pyraozlecarboxylate
Ethyl 1H-pyrazole-3-carbo...
ETHYL 1H-PYRAZOLE-3-ARBOXYLATE
EthylPyrazole-3-carboxylate>
Ethyl 2H-pyrazole-3-carboxylate
ETHYL 1H-PYRAZOLE-3-CARBOXYLATE
Ethyl 1H-pyrazole-3-carboxylate 95%
Pyrazole-5-carboxylic acid ethyl ester
Pyrazole-3-carboxylic acid, ethyl ester
1H-PYRAZOLE-3-CARBOXYLIC ACID, ETHYL ESTER
ethyl 1H-pyrazole-3-carboxylate(SALTDATA: FREE)
[Molecular Formula]

C6H8N2O2
[MDL Number]

MFCD00159643
[MOL File]

5932-27-4.mol
[Molecular Weight]

140.14
Chemical PropertiesBack Directory
[Melting point ]

158-160 °C
[Boiling point ]

279 °C
[density ]

1.214
[Fp ]

123 °C
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

powder
[pka]

11.04±0.10(Predicted)
[color ]

yellowish-orange
[InChI]

InChI=1S/C6H8N2O2/c1-2-10-6(9)5-3-4-7-8-5/h3-4H,2H2,1H3,(H,7,8)
[InChIKey]

MSPOSRHJXMILNK-UHFFFAOYSA-N
[SMILES]

N1C=CC(C(OCC)=O)=N1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37/39
[WGK Germany ]

3
[TSCA ]

No
[HazardClass ]

IRRITANT
[HS Code ]

2933199090
[Storage Class]

13 - Non Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl pyrazole-3-carboxylate(5932-27-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

5-Pyrazolecarboxylic acid

1621-91-6

Ethyl pyrazole-3-carboxylate

5932-27-4

Pyrazole-3-carboxylic acid (1.112 g, 10 mmol) was dissolved in ethanol (50 mL) at 80 °C, followed by slow addition of concentrated sulfuric acid (2 mL). The reaction mixture was kept under stirring for 2 hours. Upon completion of the reaction, ethyl 1H-pyrazole-3-carboxylate (1.350 g, 9.6 mmol, 96% yield) was obtained.

[References]

[1] Journal of the Iranian Chemical Society, 2016, vol. 13, # 5, p. 823 - 830
[2] Patent: US9206115, 2015, B2. Location in patent: Page/Page column 25-26
[3] Patent: EP3235819, 2017, A1. Location in patent: Paragraph 0264; 0265
[4] Journal of the American Chemical Society, 2000, vol. 122, # 44, p. 10810 - 10820
[5] Patent: WO2008/92942, 2008, A2. Location in patent: Page/Page column 20
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