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4,6-Diaminopyrimidine

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4,6-Diaminopyrimidine Basic information

Product Name:
4,6-Diaminopyrimidine
Synonyms:
  • (6-aminopyrimidin-4-yl)amine
  • 6-PyriMidinediaMine
  • TIMTEC-BB SBB004336
  • 4,6-DIAMINOPYRIMIDINE
  • 4,6-PYRIMIDINEDIAMINE
  • 4,6-Pyrimidinediamine (9CI)
  • PYRIMIDINE-4,6-DIAMINE
  • 4,6-Diaminopyrimidine>
CAS:
2434-56-2
MF:
C4H6N4
MW:
110.12
Product Categories:
  • Heterocycle-Pyrimidine series
  • APIs & Intermediate
  • Amines
  • Pyrimidines
  • Nucleic acids
  • PYRIMIDINE
Mol File:
2434-56-2.mol
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4,6-Diaminopyrimidine Chemical Properties

Melting point:
270-271°C
Boiling point:
364.0±22.0 °C(Predicted)
Density 
1.368±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
5.78±0.10(Predicted)
color 
White to Almost white
InChI
InChI=1S/C4H6N4/c5-3-1-4(6)8-2-7-3/h1-2H,(H4,5,6,7,8)
InChIKey
MISVBCMQSJUHMH-UHFFFAOYSA-N
SMILES
C1=NC(N)=CC(N)=N1
CAS DataBase Reference
2434-56-2(CAS DataBase Reference)
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Safety Information

HS Code 
29335990
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4,6-Diaminopyrimidine Usage And Synthesis

Chemical Properties

Yellow to light yellow crystal

Uses

4,6-Diaminopyrimidine is a compound used for the preparations of pharmaceutical goods. It was shown that organotin polyamines derived from reaction with 4,6-diaminopyrimidines displayed good inhibition of two pancreatic cancer cell lines.

Synthesis

40070-06-2

2434-56-2

General procedure for the synthesis of 4,6-diaminopyrimidine from the compound (CAS:40070-06-2): 250 mL of 11.5 mol/L hydrochloric acid solution was added to the 4,6-diamino-2-sulfinic acid pyrimidine filter cake obtained in step 2, and the mixture was cooled to -5 °C and stirred continuously for 0.5 h. The mixture was then purified to -5 °C and stirred continuously for 0.5 h. The mixture was purified to -5 °C and stirred continuously for 0.5 h. The mixture was purified to -5 °C and stirred continuously for 0.5 h. The yield of this step was 100%.

References

[1] Patent: CN103709164, 2016, B. Location in patent: Paragraph 0034; 0090; 0105; 0108
[2] Journal of the Chemical Society, 1946, p. 4106,4109
[3] Journal of the Chemical Society, 1946, p. 4106,4109

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