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Methyl 6-HydroxypyriMidine-4-carboxylate

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Products Intro: Product Name:Methyl 6-oxo-1,6-dihydropyrimidine-4-carboxylate
CAS:7399-93-1
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: CAS:7399-93-1
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Products Intro: Product Name:Methyl 6-HydroxypyriMidine-4-carboxylate
CAS:7399-93-1
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Products Intro: Product Name:Methyl 6-oxo-3,6-dihydropyrimidine-4-carboxylate
CAS:7399-93-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-44131
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Products Intro: Product Name:Methyl 6-HydroxypyriMidine-4-carboxylate
CAS:7399-93-1
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Methyl 6-HydroxypyriMidine-4-carboxylate manufacturers

Methyl 6-HydroxypyriMidine-4-carboxylate Basic information
Product Name:Methyl 6-HydroxypyriMidine-4-carboxylate
Synonyms:Methyl 6-HydroxypyriMidine-4-carboxylate;4-PyriMidinecarboxylic acid, 1,6-dihydro-6-oxo-, Methyl ester;Methyl 6-oxo-3,6-dihydropyriMidine-4-carboxylate;6-Oxo-3,6-dihydro-pyrimidine-4-carboxylic acid methyl ester;METHYL 6-HYDROXYPYRIMIDINE-4-CARBOXYLAT;methyl4-oxo-1H-pyrimidine-6-carboxylate;Methyl 6-HydroxypyriMidine-4-carboxylate ISO 9001:2015 REACH;Methyl 6-oxo-1,6-dihydropyriMidine-4-carboxylate
CAS:7399-93-1
MF:C6H6N2O3
MW:154.12
EINECS:
Product Categories:
Mol File:7399-93-1.mol
Methyl 6-HydroxypyriMidine-4-carboxylate Structure
Methyl 6-HydroxypyriMidine-4-carboxylate Chemical Properties
Boiling point 263.8±50.0 °C(Predicted)
density 1.39±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka6.88±0.40(Predicted)
AppearanceOff-white to light brown Solid
Safety Information
HS Code 2933599590
MSDS Information
Methyl 6-HydroxypyriMidine-4-carboxylate Usage And Synthesis
Synthesis
Methanol

67-56-1

6-Hydroxypyrimidine-4-carboxylic acid

6299-87-2

Methyl 6-HydroxypyriMidine-4-carboxylate

7399-93-1

Step 9A: Synthesis of methyl 6-oxo-1,6-dihydropyrimidine-4-carboxylate. 6-Hydroxy-4-pyrimidinecarboxylic acid (36.0 g, 257 mmol) was dissolved in methanol (360 mL), and chlorotrimethylsilane (56 g, 554 mmol) was slowly added dropwise. The reaction mixture was stirred at room temperature for 8 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residual solid was mixed with 200 mL of methanol and refluxed for 30 minutes. After cooling to room temperature, the precipitated solid was collected by filtration and washed with a small amount of methanol. The product was dried under vacuum at 35 °C to give 27.9 g (70% yield) of methyl 6-oxo-3,6-dihydropyrimidine-4-carboxylate.1H NMR (300 MHz, DMSO-d6) data were as follows: δ (ppm) 12.50 (broad single peak, 1H), 8.23 (single peak, 1H), 6.83 (single peak, 1H), 3.80 (single peak, 3H).

References[1] Patent: US2009/111821, 2009, A1. Location in patent: Page/Page column 23
Methyl 6-HydroxypyriMidine-4-carboxylate Preparation Products And Raw materials
Raw materials6-Hydroxypyrimidine-4-carboxylic acid-->Chlorotrimethylsilane-->Methanol
Preparation Productsmethyl 6-chloropyrimidine-4-carboxylate
Tag:Methyl 6-HydroxypyriMidine-4-carboxylate(7399-93-1) Related Product Information
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