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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Nitro-pyrimidine >  ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE

ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE

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ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE Basic information

Product Name:
ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE
Synonyms:
  • ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE
  • 2,6-dichloro-5-nitropyrimidine-4-carboxylic acid ethyl ester
  • 2,6-Dichloro-4-(ethoxycarbonyl)-5-nitropyrimidine
  • 4-Pyrimidinecarboxylic acid, 2,6-dichloro-5-nitro-, ethyl ester
  • ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE ISO 9001:2015 REACH
CAS:
54368-61-5
MF:
C7H5Cl2N3O4
MW:
266.04
Product Categories:
  • Pyrimidine series
Mol File:
Mol File
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ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE Chemical Properties

Melting point:
36-38°C
Boiling point:
391.4±37.0 °C(Predicted)
Density 
1.602
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
pka
-9.02±0.39(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

Hazard Codes 
Xi
HS Code 
2933599590
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ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATE Usage And Synthesis

Uses

Ethyl 2,6-Dichloro-5-nitropyrimidine-4-carboxylate is a useful chemical compound for preparation of pyrimidinediamines as IgE and/or IgG receptor modulators.

Synthesis

Ethyl ethyl 2,6-dihydroxy-5-nitropyrimidine-4-carboxylate was dissolved in acetonitrile (50 mL), stirred at room temperature for 30 minutes, trichlorophosphorus was added, warmed to reflux, and the reaction was carried out for 30 minutes, and the progress of the reaction was detected by thin layer chromatography. At the end of the reaction, cooled to room temperature, poured into ice water, stirred, extracted with dichloromethane (50mL??3), the organic phase was washed with saturated sodium bicarbonate solution, decolorized by activated charcoal and dried with anhydrous sodium sulfate, filtered, concentrated and then added isopropanol (30mL), heated to dissolve, stirred, a white solid precipitated, left to stand for 2h, filtered, filter cake was dried to obtain the target compound 2,6-dichloro-5- Nitropyrimidine-4-carboxylic acid ethyl ester.

ETHYL 2,6-DICHLORO-5-NITROPYRIMIDINE-4-CARBOXYLATESupplier

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