Basic information Safety Supplier Related

5-CHLORO-1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID

Basic information Safety Supplier Related

5-CHLORO-1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID Basic information

Product Name:
5-CHLORO-1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID
Synonyms:
  • 5-Chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylicacid97%
  • 5-Chloro-1-methyl-3-(trifluoromethyl)
  • BUTTPARK 99\18-36
  • 5-CHLORO-1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID
  • RARECHEM AL BO 1764
  • 4-Carboxy-5-chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole
  • 5-chloro-1-methyl-3-trifluoromethylpyrazole-4-carboxylic acid
  • 1H-Pyrazole-4-carboxylic acid, 5-chloro-1-methyl-3-(trifluoromethyl)-
CAS:
128455-63-0
MF:
C6H4ClF3N2O2
MW:
228.56
EINECS:
671-543-4
Product Categories:
  • Carboxylic Acids
  • Pyrazoles & Triazoles
  • Heterocyclic Building Blocks
  • New Products for Chemical Synthesis
  • Pyrazoles
  • Building Blocks
  • Pyrazole
  • Chemical Synthesis
  • Carboxylic Acids
  • Pyrazoles & Triazoles
  • C6
Mol File:
128455-63-0.mol
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5-CHLORO-1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID Chemical Properties

Melting point:
201 °C
Boiling point:
284.4±40.0 °C(Predicted)
Density 
1.71±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
1.77±0.50(Predicted)
CAS DataBase Reference
128455-63-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26
HazardClass 
IRRITANT
HS Code 
2933199090
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5-CHLORO-1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID Usage And Synthesis

Synthesis

128455-62-9

128455-63-0

Example 5: 10 g of 5-chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxaldehyde was added to 50 mL of an aqueous solution containing 5 g of sodium hydroxide (2 equivalents). Under vigorous stirring, 34.4 g of 35% hydrogen peroxide solution was slowly added in 8 drops over a temperature range of 40°C to 50°C, taking 1.5 hours. After the dropwise addition was completed, the reaction mixture was continued to be stirred for 30 minutes and subsequently cooled to 15°C. The pH of the reaction solution was adjusted to 1 with concentrated hydrochloric acid and the solid product was precipitated. The crystals were collected by filtration and washed well with water, after which the crystals were dissolved in ether. The ether solution was dried over anhydrous magnesium sulfate and decolorized by activated carbon, and then the ether was removed by distillation under reduced pressure to give 8.6 g of 5-chloro-1-methyl-3-(trifluoromethyl)pyrrole-4-carboxylic acid in 80.0% yield and 197.5-199.5 °C melting point.

References

[1] Patent: US2004/19221, 2004, A1. Location in patent: Page 7
[2] Patent: CN103951663, 2016, B. Location in patent: Paragraph 0091; 0096; 0097
[3] Journal of Heterocyclic Chemistry, 1990, vol. 27, # 2, p. 243 - 245
[4] Patent: WO2007/84868, 2007, A2. Location in patent: Page/Page column 39
[5] Journal of Heterocyclic Chemistry, 2011, vol. 48, # 2, p. 389 - 396

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