Basic information Safety Supplier Related

5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID

Basic information Safety Supplier Related

5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID Basic information

Product Name:
5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID
Synonyms:
  • 5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID
  • 3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid
  • Albb-005389
  • 3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)
  • 3-Carboxy-5-(trifluoromethyl)-1H-pyrazole
  • 1H-Pyrazole-3-carboxylic acid, 5-(trifluoromethyl)-
  • 5-Trifluoromethylpyrazole-3-carboxylic acid
  • 3-(Trifluoromethyl)pyrazole-5-carboxylic Acid
CAS:
129768-28-1
MF:
C5H3F3N2O2
MW:
180.08
Product Categories:
  • pharmacetical
Mol File:
129768-28-1.mol
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5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID Chemical Properties

Melting point:
171 - 172°C
Boiling point:
354.2±42.0 °C(Predicted)
Density 
1.682±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
3.55±0.10(Predicted)
color 
White to Off-White
InChI
InChI=1S/C5H3F3N2O2/c6-5(7,8)3-1-2(4(11)12)9-10-3/h1H,(H,9,10)(H,11,12)
InChIKey
CIVNBJPTGRMGRS-UHFFFAOYSA-N
SMILES
N1C(C(F)(F)F)=CC(C(O)=O)=N1
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-20/21/22
Safety Statements 
36/37
HazardClass 
IRRITANT
HS Code 
29331990
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5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID Usage And Synthesis

Chemical Properties

Off-white solid

Synthesis

881693-05-6

129768-28-1

General procedure for the synthesis of 5-trifluoromethylpyrazole-3-carboxylic acid from 1-benzyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid: liquid ammonia (ca. 50 mL) was condensed into a three-necked flask in an ethanol-dry ice bath, followed by the addition of 1-benzyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid (100 mg, 3.70 mmol). Sodium metal (about 260 mg, 11.3 mmol) was added to the reaction mixture in batches until the reaction solution showed a persistent blue color for more than 5 minutes. Upon completion of the reaction, the ammonia was allowed to evaporate naturally overnight. Water was added to the residue and acidified with 2N HCl solution to pH < 7. The aqueous phase was extracted twice with ethyl acetate, the organic phases were combined and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give 5-trifluoromethyl-2H-pyrazole-3-carboxylic acid (560 mg, 3.11 mmol, 84% yield) as a yellow solid with mass spectral data of MS m/z = 179.0 (API-). The product could be used in subsequent reactions without further purification.

References

[1] Patent: WO2007/68465, 2007, A1. Location in patent: Page/Page column 30
[2] Patent: US2006/69145, 2006, A1. Location in patent: Page/Page column 9; 14

5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID Preparation Products And Raw materials

Raw materials

5-TRIFLUOROMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACIDSupplier

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