2-Amino-4-(trifluoromethyl)pyrimidine
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
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)
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
- Ⅲ
- HS Code
- 29335990
MSDS
- Language:English Provider:ALFA
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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