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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Bromopyrimidine >  5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE

5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE

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5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE Basic information

Product Name:
5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE
Synonyms:
  • 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE
  • 5-Bromo-2-chloro-4-(methylsulphanyl)pyrimidine
  • 5-Bromo-2-chloro-4-(methylsulfanyl)pyrimidine
  • 5-Bromo-2-chloro-4-(methylsulphanyl)pyrimidine, 5-Bromo-2-chloro-4-(methylthio)-1,3-diazine
  • 5-Bromo-2-chloro-4-(methylthio)
  • Pyrimidine, 5-bromo-2-chloro-4-(methylthio)-
  • 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE ISO 9001:2015 REACH
  • 5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDIN
CAS:
59549-51-8
MF:
C5H4BrClN2S
MW:
239.52
Product Categories:
  • Building Blocks
  • Pyrimidine
Mol File:
59549-51-8.mol
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5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE Chemical Properties

Melting point:
56-58℃
Boiling point:
346.1±27.0 °C(Predicted)
Density 
1.83
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
-1.87±0.29(Predicted)
Appearance
White to light yellow Solid
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2933599590
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5-BROMO-2-CHLORO-4-(METHYLTHIO)PYRIMIDINE Usage And Synthesis

Synthesis

36082-50-5

5188-07-8

59549-51-8

General procedure for the preparation of 5-bromo-2-chloro-4-(methylthio)pyrimidine: 2 g of sodium methanethiol (28.5 mmol, 1 eq.) and 6.5 g of 5-bromo-2,4-dichloropyrimidine (28.5 mmol, 1 eq.) were reacted at room temperature with stirring for 24 hr in 50 mL of anhydrous acetonitrile. Upon completion of the reaction, the mixture was poured into water and extracted with dichloromethane, the organic phase was dried over anhydrous sodium sulfate and subsequently concentrated under reduced pressure to remove the solvent. The crude product was purified by recrystallization from hexane to give 4 g of the target compound (70% yield).1H-NMR (400 MHz, CDCl3) data: δ 8.31 (s, 1H), 2.59 (s, 3H).

References

[1] Patent: EP1878726, 2008, A1. Location in patent: Page/Page column 36
[2] Patent: US2008/176866, 2008, A1. Location in patent: Page/Page column 8
[3] Patent: WO2007/71455, 2007, A1. Location in patent: Page/Page column 252-253
[4] Patent: US2007/232632, 2007, A1. Location in patent: Page/Page column 109
[5] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 22, p. 6206 - 6211

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