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5-Bromo-2-methoxypyrimidine

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5-Bromo-2-methoxypyrimidine Basic information

Product Name:
5-Bromo-2-methoxypyrimidine
Synonyms:
  • Bromomethoxypyrimidine
  • 5-BROMO-2-METHOXYPYRIMIDINE 97
  • 2-Methoxy-5-bromopyrimidine
  • 5-Bromo-2-methoxypyrimidine
  • 5-Bromo-2-methoxy-1,3-diazine
  • 5-Bromo-2-methoxypyrimidine 98%
  • 2-Methoxy-5-broMopyriMidine(5-BroMo-2-MethoxypyriMidine)
  • 5-Bromo-22-methoxypyrimidine
CAS:
14001-66-2
MF:
C5H5BrN2O
MW:
189.01
EINECS:
626-366-7
Product Categories:
  • Heterocycle-Pyrimidine series
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyrimidines
  • PyrimidinesHeterocyclic Building Blocks
  • Pyrimidine
  • Alkoxy
  • Organohalides
Mol File:
14001-66-2.mol
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5-Bromo-2-methoxypyrimidine Chemical Properties

Melting point:
55.5-59.5 °C (lit.)
Boiling point:
259.8±32.0 °C(Predicted)
Density 
1.628±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
-0.22±0.22(Predicted)
form 
Solid
color 
White to yellow (may have pinkish tinge)
CAS DataBase Reference
14001-66-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-43
Safety Statements 
37/39
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29333990
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5-Bromo-2-methoxypyrimidine Usage And Synthesis

Chemical Properties

White solid

Synthesis

124-41-4

32779-36-5

14001-66-2

Synthesis of compound 11-3 (5-bromo-2-methoxypyrimidine): to a solution of 5-bromo-2-chloropyrimidine (11-2, 2.0 g, 10 mmol) in methanol (15 mL) was added sodium methanolate (CH3ONa, 2.16 g, 40 mmol). The reaction mixture was stirred at 70 °C overnight. Upon completion of the reaction, methanol was removed by rotary evaporator under reduced pressure. Water (10 mL) was slowly added to the residue, followed by extraction with ethyl acetate (300 mL x 3). The organic phases were combined, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated to give 11-3 as a yellow solid (1.17 g, 60% yield).

References

[1] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 289-290
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 19, p. 5849 - 5853

5-Bromo-2-methoxypyrimidine Preparation Products And Raw materials

Raw materials

Preparation Products

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