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2-Amino-4-(trifluoromethyl)pyrimidine

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2-Amino-4-(trifluoromethyl)pyrimidine Basic information

Product Name:
2-Amino-4-(trifluoromethyl)pyrimidine
Synonyms:
  • 2-AMINO-4-(TRIFLUOROMETHYL)PYRIMIDINE
  • 4-(TRIFLUOROMETHYL)PYRIMIDIN-2-AMINE
  • 4-(TRIFLUOROMETHYL)PYRIMIDIN-2-YLAMINE
  • AKOS B024896
  • ART-CHEM-BB B024896
  • BUTTPARK 27\08-65
  • 2-Amino-4-(trifluoromethyl)pyrimdine
  • 2-Amino-4-(trifluoromethyl)pyrimidine 97%
CAS:
16075-42-6
MF:
C5H4F3N3
MW:
163.1
EINECS:
623-256-0
Product Categories:
  • Fluorine series
  • Imidazoles & Benzimidazoles
  • Pyrazines, Pyrimidines & Pyridazines
  • Pyrimidine series
  • Amines
  • Pyrazines, Pyrimidines & Pyridazines
  • Imidazoles & Benzimidazoles
Mol File:
16075-42-6.mol
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2-Amino-4-(trifluoromethyl)pyrimidine Chemical Properties

Melting point:
175-177°C
Boiling point:
260.7±50.0 °C(Predicted)
Density 
1.460±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
1.90±0.10(Predicted)
color 
White to Light yellow
λmax
308nm(EtOH aq.)(lit.)
CAS DataBase Reference
16075-42-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,N,T
Risk Statements 
36/37/38-50-43-36-25
Safety Statements 
26-36/37/39-61-45-36/37
RIDADR 
2811
WGK Germany 
3
HazardClass 
IRRITANT
PackingGroup 
HS Code 
29335990

MSDS

  • Language:English Provider:ALFA
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2-Amino-4-(trifluoromethyl)pyrimidine Usage And Synthesis

Chemical Properties

White to brown powder

Synthesis

59938-06-6

113-00-8

16075-42-6

Step 2: To a solution of compound [63] (22.8 g, 2.4 mmol, 1 eq.) in anhydrous ethanol (100 mL), NaOH granules (9.55 g, 238 mmol, 1 eq.) were added and the reaction mixture was stirred for 16 h at room temperature. Subsequently, a solution of compound [84] was slowly added through a dropping funnel over a period of 2 hours. After addition, the reaction mixture was continued to be stirred for 2 hours. Upon completion of the reaction, the solvent was removed by evaporation and the residue was dissolved in water (500 mL) with vigorous stirring for 2 hours, followed by standing at room temperature overnight. The precipitate precipitated was collected by filtration and dried under vacuum to give compound [85] as a light yellow solid (20.6 g, 53% yield).

References

[1] Patent: WO2014/16849, 2014, A2. Location in patent: Page/Page column 117

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