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4,6-Diaminopyrimidine

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Products Intro: Product Name:4,6-Diaminopyrimidine
CAS:2434-56-2
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CAS:2434-56-2
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CAS:2434-56-2
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Products Intro: Product Name:4,6-Diaminopyrimidine
CAS:2434-56-2
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4,6-Diaminopyrimidine manufacturers

  • 4,6-Diaminopyrimidine
  • 4,6-Diaminopyrimidine  pictures
  • $1.10 / 1g
  • 2025-11-18
  • CAS:2434-56-2
  • Min. Order: 1g
  • Purity: 99.00%
  • Supply Ability: 100 Tons Min
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
EINECS:
Product Categories:Heterocycle-Pyrimidine series;APIs & Intermediate;Amines;Pyrimidines;Nucleic acids;PYRIMIDINE
Mol File:2434-56-2.mol
4,6-Diaminopyrimidine Structure
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
pka5.78±0.10(Predicted)
color White to Almost white
InChIInChI=1S/C4H6N4/c5-3-1-4(6)8-2-7-3/h1-2H,(H4,5,6,7,8)
InChIKeyMISVBCMQSJUHMH-UHFFFAOYSA-N
SMILESC1=NC(N)=CC(N)=N1
CAS DataBase Reference2434-56-2(CAS DataBase Reference)
Safety Information
HS Code 29335990
MSDS Information
4,6-Diaminopyrimidine Usage And Synthesis
Chemical PropertiesYellow to light yellow crystal
Uses4,6-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
NSC54047

40070-06-2

4,6-Diaminopyrimidine

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
Tag:4,6-Diaminopyrimidine(2434-56-2) Related Product Information
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