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2-aminopropanediamide

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2-aminopropanediamide Basic information

Product Name:
2-aminopropanediamide
Synonyms:
  • 2-aminopropanediamide
  • Aminomalonamide
  • 2-azanylpropanediamide
  • favipiravir-001
  • NSC 75208
  • PropanediaMide, 2-aMino-
  • 2-Aminopropane-1,3-diamide
  • amino-malonic acid diamide
CAS:
62009-47-6
MF:
C3H7N3O2
MW:
117.11
EINECS:
263-370-4
Product Categories:
  • Miscellaneous Reagents
  • Amines
  • Intermediates
Mol File:
62009-47-6.mol
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2-aminopropanediamide Chemical Properties

Melting point:
180-185°C
Boiling point:
410.1±40.0 °C(Predicted)
Density 
1.399±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
DMSO (Sparingly), Methanol (Sparingly)
pka
9.87±0.70(Predicted)
form 
Solid
color 
Pale Yellow to Beige
InChI
InChI=1S/C3H7N3O2/c4-1(2(5)7)3(6)8/h1H,4H2,(H2,5,7)(H2,6,8)
InChIKey
GFQBSQXXHYLABK-UHFFFAOYSA-N
SMILES
C(N)(=O)C(N)C(N)=O
CAS DataBase Reference
62009-47-6
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Safety Information

HS Code 
2924190090
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2-aminopropanediamide Usage And Synthesis

Chemical Properties

Beige Solid

Uses

2-aminopropanediamide is a reagent used in the synthesis of Imidazole derivatives.

Synthesis

6829-40-9

62009-47-6

The general procedure for the synthesis of 2-aminomalonamide from diethyl aminomalonate is as follows: 17.5 g of diethyl 2-aminomalonate and 22 g of 50% aqueous ammonium chloride were accurately weighed, mixed, and then heated at reflux for 2 h at 100 °C. The reaction was completed by filtration. After completion of the reaction, the reaction mixture was cooled to room temperature and the solid product was separated by filtration. The resulting solid was dried with hot air at 60 °C for 8 h. A white crystalline powder 2-aminomalonamide 10.2 g was obtained in 87% yield.

References

[1] Patent: WO2007/144686, 2007, A1. Location in patent: Page/Page column 129-130
[2] Patent: CN108250104, 2018, A. Location in patent: Paragraph 0016; 0017; 0018; 0019
[3] Patent: EP2196460, 2010, A1. Location in patent: Page/Page column 5; 6
[4] Journal of the American Chemical Society, 1949, vol. 71, p. 78,79, 80

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