5-CHLORO-3-TRIFLUOROMETHYL-1H-PYRAZOLE
- Product Name
- 5-CHLORO-3-TRIFLUOROMETHYL-1H-PYRAZOLE
- CAS No.
- 1003320-19-1
- Chemical Name
- 5-CHLORO-3-TRIFLUOROMETHYL-1H-PYRAZOLE
- Synonyms
- 5-Chloro-3-(trifluoromethyl)pyrazole;5-CHLORO-3-TRIFLUOROMETHYL-1H-PYRAZOLE;1H-Pyrazole, 3-chloro-5-(trifluoromethyl)-
- CBNumber
- CB6814030
- Molecular Formula
- C4H2ClF3N2
- Formula Weight
- 170.52
- MOL File
- Mol file
5-CHLORO-3-TRIFLUOROMETHYL-1H-PYRAZOLE Property
- Boiling point:
- 214.4±35.0 °C(Predicted)
- Density
- 1.602±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 7.60±0.10(Predicted)
- Appearance
- White to off-white Solid
Safety
- HS Code
- 2933199090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
5-CHLORO-3-TRIFLUOROMETHYL-1H-PYRAZOLE Chemical Properties,Usage,Production
Synthesis
922516-22-1
131797-35-8
The general procedure for the synthesis of 5-chloro-N,N-dimethyl-3-(trifluoromethyl)-1H-pyrazole-1-sulfonamide from 5-chloro-N,N-dimethyl-3-(trifluoromethyl)-1H-pyrazole is as follows: 5-chloro-N,N-dimethyl-3-(trifluoromethyl)-1H-pyrazole-1-sulfonamide (8.0 g, 29 mmol) was dissolved in a reaction system at 0°C with trifluoroacetic acid (TFA, 11 mL. 140 mmol) were co-dissolved in the reaction system. Subsequently, the reaction mixture was stirred continuously at room temperature overnight. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure and the resulting residue was diluted with ethyl acetate (EtOAc, 50 mL) and washed with water (50 mL). The aqueous layer was further extracted with ethyl acetate (2 x 50 mL). All organic phases were combined, dried with anhydrous sodium sulfate (Na2SO4), filtered into a round bottom flask and finally concentrated under reduced pressure to afford the target product 5-chloro-3-trifluoromethyl-1H-pyrazole (5.0 g, 29 mmol, 100% yield). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6) with chemical shift δppm 6.97 (s, 1H).
References
[1] Patent: WO2014/152738, 2014, A1. Location in patent: Page/Page column 67
[2] Patent: WO2015/52226, 2015, A1. Location in patent: Paragraph 0452
[3] Patent: WO2008/91594, 2008, A2. Location in patent: Page/Page column 90
[4] Patent: US2010/240619, 2010, A1. Location in patent: Page/Page column 64
[5] Journal of Medicinal Chemistry, 2016, vol. 59, # 6, p. 2760 - 2779
5-CHLORO-3-TRIFLUOROMETHYL-1H-PYRAZOLE Preparation Products And Raw materials
Raw materials
Preparation Products
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