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2-Amino-4-(trifluoromethyl)pyrimidine

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CAS:16075-42-6
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Products Intro: Product Name:2-amino-4-trifluoromethylpyrimidine
CAS:16075-42-6
Purity:98% Package:1KG;10KG;50KG

2-Amino-4-(trifluoromethyl)pyrimidine manufacturers

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 Structure
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
pka1.90±0.10(Predicted)
color White to Light yellow
λmax308nm(EtOH aq.)(lit.)
InChI1S/C5H4F3N3/c6-5(7,8)3-1-2-10-4(9)11-3/h1-2H,(H2,9,10,11)
InChIKeyNKOTXYPTXKUCDL-UHFFFAOYSA-N
SMILESNc1nccc(n1)C(F)(F)F
CAS DataBase Reference16075-42-6(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 
HS Code 29335990
Storage Class6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard ClassificationsAcute Tox. 2 Oral
Aquatic Acute 1
Eye Irrit. 2
Resp. Sens. 1
MSDS Information
ProviderLanguage
ALFA English
2-Amino-4-(trifluoromethyl)pyrimidine Usage And Synthesis
Chemical PropertiesWhite to brown powder
Synthesis
1-Ethoxy-3-trifluoromethyl-1,3-butadiene

59938-06-6

guanidine

113-00-8

2-Amino-4-(trifluoromethyl)pyrimidine

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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