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4-Hydroxy-6-aminopyrimidine

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4-Hydroxy-6-aminopyrimidine Basic information

Product Name:
4-Hydroxy-6-aminopyrimidine
Synonyms:
  • 4(3H)-Pyrimidinone, 6-amino-
  • 4-AMINO-6-HYDROXYPYRIMIDINE
  • 6-AMINOPYRIMIDIN-4(3H)-ONE
  • 6-AMINOPYRIMIDIN-4-OL
  • 6-amino-1H-pyrimidin-4-one
  • 4(1H)-Pyrimidinone, 6-amino- (8CI,9CI)
  • 6-Amino-3H-pyrimidin-4-one
  • 4(1H)-Pyrimidinone, 6-amino-
CAS:
1193-22-2
MF:
C4H5N3O
MW:
111.1
EINECS:
214-771-8
Product Categories:
  • Bases & Related Reagents
  • Heterocycles
  • Nucleotides
  • Heterocycle-Pyrimidine series
  • Pyridines, Pyrimidines, Purines and Pteredines
  • PYRIMIDINE
  • Fluorobenzene
  • Heterocyclic Compounds
  • Nucleotides and Nucleosides
  • Pyrimidines
Mol File:
1193-22-2.mol
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4-Hydroxy-6-aminopyrimidine Chemical Properties

Melting point:
262-264°C
Boiling point:
227.5±43.0 °C(Predicted)
Density 
1.55±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO
form 
Solid
pka
10.04±0.40(Predicted)
color 
White
BRN 
112429
InChI
InChI=1S/C4H5N3O/c5-3-1-4(8)7-2-6-3/h1-2H,(H3,5,6,7,8)
InChIKey
HFMLLTVIMFEQRE-UHFFFAOYSA-N
SMILES
C1=NC(N)=CC(=O)N1
CAS DataBase Reference
1193-22-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-41
Safety Statements 
26-36-39
HazardClass 
IRRITANT
HS Code 
2933599590

MSDS

  • Language:English Provider:ALFA
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4-Hydroxy-6-aminopyrimidine Usage And Synthesis

Chemical Properties

White Solid

Synthesis

1004-40-6

1193-22-2

Step 2: 2-mercapto-4-amino-6-hydroxypyridine (mass ratio 1:15) was added to 25% ammonia, followed by the addition of activated nickel and titanium dioxide, wherein the molar ratio of 2-mercapto-4-amino-6-hydroxypyridine, activated nickel and titanium dioxide was 1:4:1.5. The mixture was heated to 90°C and the reaction was carried out at reflux for 5 hours. Upon completion of the reaction, the activated nickel and titanium dioxide were removed by thermal filtration. The filtrate was cooled to room temperature and the solid product was precipitated. The solid was washed with 30 mL of water and dried at 40 °C to afford 4-amino-6-hydroxypyrimidine in 98.4% yield.

References

[1] Patent: CN105218554, 2016, A. Location in patent: Paragraph 0023
[2] Journal of Medicinal Chemistry, 2002, vol. 45, # 9, p. 1918 - 1929
[3] Patent: EP1406911, 2016, B1. Location in patent: Paragraph 00382; 00383

4-Hydroxy-6-aminopyrimidine Preparation Products And Raw materials

Raw materials

4-Hydroxy-6-aminopyrimidineSupplier

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