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2 4-Dichloro-5-methylpyrimidine(CAS# 1780-31-0)

Chemical Property:

Molecular Formula C5H4Cl2N2
Molar Mass 163
Density 1.39 g/mL at 25 °C (lit.)
Melting Point 26-28 °C (lit.)
Boling Point 108-109 °C/11 mmHg (lit.)
Flash Point >230°F
Solubility Soluble in chloroform, ether, ethyl acetate and toluene
Vapor Presure 0.079mmHg at 25°C
Appearance powder to lump to clear liquid
Color White or Colorless to Almost white or Almost colorless
pKa -2.44±0.29(Predicted)
Storage Condition Inert atmosphere,2-8°C

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Risk and Safety

Hazard Symbols C – Corrosive
Risk Codes 34 – Causes burns
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection.
S45 – In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S27 – Take off immediately all contaminated clothing.
UN IDs UN 3261 8/PG 2
WGK Germany 3
TSCA Yes
HS Code 29335990
Hazard Class 8
Packing Group III

2 4-Dichloro-5-methylpyrimidine(CAS# 1780-31-0) Information

Use 2, 4-dichloro-5-methylpyrimidine can be used in the preparation of 2-fluoro-5-trifluoromethylpyrimidine. 2-fluoro-5-trifluoromethylpyrimidine is an important intermediate for the synthesis of pharmaceuticals, which can be used to synthesize fused ring dihydrofuran compounds, and fused ring dihydrofuran compounds can be used as G protein coupled receptor GPR119 modulators, for the treatment of diabetes, obesity and dyslipidemia disease. In addition, 2-fluoro-5-trifluoromethylpyrimidine can also be used as an intermediate in the synthesis of drugs for the treatment of Alzheimer’s disease and schizophrenia.
preparation 5-methyluracil 75g(0.59mol), phosphorus oxychloride 236g, triethylamine hydrochloride 16.5g(0.12mol), added to the reaction flask, heated to 100 ℃ ~ 110 ℃, Reflux reaction 5H, cooled to 40 ℃, add phosphorus pentachloride 248(1.19mol), heat preservation reaction 2H. After completion of the reaction, phosphorus oxychloride was recovered by distillation under reduced pressure, and distillation under reduced pressure was continued to obtain 88g(0.54mol) of 2, 4-dichloro-5-methylpyrimidine in a yield of 91.5%.

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