ChemicalBook--->CAS DataBase List--->343-67-9

343-67-9

343-67-9 Structure

343-67-9 Structure
IdentificationBack Directory
[Name]

ETHYL 4-HYDROXY-2-(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLATE
[CAS]

343-67-9
[Synonyms]

Ethyl 2-trifluoromethyl-4-oxopyrimidine-5-carboxylate
ethyl6-oxo-2-(trifluoromethyl)-1H-pyrimidine-5-carboxylate
ETHYL 4-HYDROXY-2-(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLATE
ethyl 4-hydroxy-2-(trifluoromethyl)-5-pyrimidinecarboxylate
ethyl 6-oxo-2-(trifluoromethyl)-1,6-dihydropyrimidine-5-carb...
Ethyl 4-hydroxy-2-(trifluoromethyl)pyrimidine-5-carboxylate ,97%
ethyl 6-oxo-2-(trifluoroMethyl)-1,6-dihydropyriMidine-5-carboxylate
4-Hydroxy-2-trifluoromethyl-pyrimidine-5-carboxylic acid ethyl ester
ETHYL 4-HYDROXY-2-(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLATE ISO 9001:2015 REACH
5-Pyrimidinecarboxylic acid, 1,6-dihydro-6-oxo-2-(trifluoromethyl)-, ethyl ester
5-(Ethoxycarbonyl)-4-hydroxy-2-(trifluoromethyl)pyrimidine, 5-(Ethoxycarbonyl)-4-hydroxy-2-(trifluoromethyl)-1,3-diazine
[Molecular Formula]

C8H7F3N2O3
[MDL Number]

MFCD01571344
[MOL File]

343-67-9.mol
[Molecular Weight]

236.148
Chemical PropertiesBack Directory
[Melting point ]

315-316°
[density ]

1.50
[storage temp. ]

2-8°C
[pka]

4.75±0.50(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

48-20/21/22
[Safety Statements ]

3/7/9-37/39
[HazardClass ]

IRRITANT
[HS Code ]

29335990
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Uses]

Ethyl 4-Hydroxy-2-(trifluoromethyl)pyrimidine-5-carboxylate is a useful reagent in the study of NF-κB and AP-1 gene inhibitors.
[Synthesis]

Water

7732-18-5

Diethyl ethoxymethylenemalonate

87-13-8

ETHYL 4-HYDROXY-2-(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLATE

343-67-9

Diethyl ethoxymethylenemalonate (35.0 g, 162 mmol) and trifluoroacetic acid (18 g, 162 mmol) were used as raw materials, which were dissolved in ethanol (200 mL) and sodium ethoxide (11.0 g, 162 mmol) was added. The reaction mixture was heated to reflux for 6 hours. After completion of the reaction, the reaction mixture was concentrated and water (48 mmol) was added. The resulting solid was collected by filtration, washed sequentially with ether (300 mL) and water (200 mL), and dried to give ethyl 4-hydroxy-2-trifluoromethylpyrimidine-5-carboxylate (21 g, 50% yield). The melting point of the product was >220 °C (decomposition); 1H NMR (DMSO-d6) δ 8.38,4.16 (q, 2H), 1.25 (q, 3H).

[References]

[1] Patent: US5935966, 1999, A
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