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4,6-Dihydroxy-5-formylpyrimidine

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4,6-Dihydroxy-5-formylpyrimidine Basic information

Product Name:
4,6-Dihydroxy-5-formylpyrimidine
Synonyms:
  • 4,6-DIHYDROXY-5-FORMYLPYRIMIDINE
  • 5-Pyrimidinecarboxaldehyde, 1,4-dihydro-6-hydroxy-4-oxo- (9CI)
  • (5E)-5-(Hydroxymethylidene)-1H-pyrimidine-4,6-dione
  • 1,4-Dihydro-6-hydroxy-4-oxo-5-pyrimidinecarboxaldehyde
  • 5-Pyrimidinecarboxaldehyde, 1,6-dihydro-4-hydroxy-6-oxo-
  • 4,6-Dihydroxy-5-formylpyrimidine ISO 9001:2015 REACH
  • 1,6-Dihydro-4-hydroxy-6-oxo-5-pyrimidinecarboxaldehyde
  • 1,6-Dihydro-4-hydroxy-6-oxo-pyrimidine-5-carbaldehyde
CAS:
14256-99-6
MF:
C5H4N2O3
MW:
140.1
Product Categories:
  • PYRIMIDINE
  • Heterocycle-Pyrimidine series
Mol File:
14256-99-6.mol
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4,6-Dihydroxy-5-formylpyrimidine Chemical Properties

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Off-white to light yellow Solid
CAS DataBase Reference
14256-99-6(CAS DataBase Reference)
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4,6-Dihydroxy-5-formylpyrimidine Usage And Synthesis

Synthesis

15263-75-9

14256-99-6

The general procedure for the synthesis of 4,6-dihydroxy-5-formylpyrimidines from N-((4-hydroxy-6-oxo-1,6-dihydropyrimidin-5-yl)methylene)-N-methylmethylammonium chloride was as follows: 30 mL of water was added to the reaction flask and stirring was initiated. The temperature of the reaction system was raised to 20-30 °C, followed by the addition of N-((4,6-dihydroxypyrimidin-5-yl)methylene)-N-methylmethylammonium chloride salt (10.0 g, 49.11 mmol). The reaction was kept at this temperature for 18 hours. After completion of the reaction, 50 mL of anhydrous ethanol was added to the mixture and stirring was continued. The reaction mixture was filtered and the resulting filter cake was washed with a small amount of anhydrous ethanol. Finally, the product was dried under vacuum at 40-45 °C to give 5.77 g of yellow solid.

References

[1] Patent: CN108178748, 2018, A. Location in patent: Paragraph 0051; 0052; 0063-0065

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