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2-(methylthio)pyrimidine-4,6-diol

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2-(methylthio)pyrimidine-4,6-diol Basic information

Product Name:
2-(methylthio)pyrimidine-4,6-diol
Synonyms:
  • 4-Hydroxy-2-(methylthio)pyrimidin-6(1H)-one, 4,6-Dihydroxy-2-(methylthio)pyrimidine, 2-(Methylsulphanyl)pyrimidine-4,6-diol
  • 6-Hydroxy-2-(methylthio)pyrimidin-4(3H)-one
  • 6-Hydroxy-2-(Methylthio)-4-pyriMidinone
  • NSC 44557
  • 2-Methylthio-4,6-pyriMidinedione, 95+%
  • S-MTBA
  • S-METHYLTHIOBARBITURIC ACID
  • 2-(Methylmercapto)-4,6-pyrimidinediol
CAS:
1979-98-2
MF:
C5H6N2O2S
MW:
158.18
EINECS:
217-839-5
Product Categories:
  • Pyrimidine
  • Bases & Related Reagents
  • Nucleotides
  • Sulfur & Selenium Compounds
  • Nucleotides and Nucleosides
  • Pyrimidines
  • Heterocycle-Pyrimidine series
Mol File:
1979-98-2.mol
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2-(methylthio)pyrimidine-4,6-diol Chemical Properties

Melting point:
>300 °C(lit.)
Density 
1.55±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Ethyl Acetate, Ethanol, Methanol
form 
Powder
pka
4.06±0.10(Predicted)
color 
White
CAS DataBase Reference
1979-98-2(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
2
HS Code 
29339900

MSDS

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2-(methylthio)pyrimidine-4,6-diol Usage And Synthesis

Chemical Properties

White Solid

Uses

2-(Methylthio)-4,6-pyrimidinediol (cas# 1979-98-2) is a compound useful in organic synthesis.

Synthesis

504-17-6

74-88-4

1979-98-2

Step a: Synthesis of 2-methylthio-pyrimidine-4,6-diol (19a); Iodomethane (32.64 g, 220 mmol) was slowly added dropwise to a suspension of thiobarbituric acid (29 g, 200 mmol) dissolved in ethanol (300 mL) and 2M aqueous sodium hydroxide (110 mL) at room temperature. The reaction mixture was stirred overnight at room temperature, followed by warming to 60 °C and continued stirring for 2 hours. Upon completion of the reaction, ethanol was removed by distillation under reduced pressure, an appropriate amount of water was added and the mixture was cooled in an ice bath for 2 hours. The precipitated solid 4,6-dihydroxy-2-methylmercaptopyrimidine was collected by filtration, washed with ice water and dried to give the product (30 g, 95% yield).

References

[1] Patent: WO2008/95999, 2008, A1. Location in patent: Page/Page column 96
[2] Patent: WO2012/97478, 2012, A1. Location in patent: Page/Page column 58-59

2-(methylthio)pyrimidine-4,6-diol Preparation Products And Raw materials

Raw materials

Preparation Products

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