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5-Methyl-1,3,4-oxadiazol-2(3H)-one

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5-Methyl-1,3,4-oxadiazol-2(3H)-one Basic information

Product Name:
5-Methyl-1,3,4-oxadiazol-2(3H)-one
Synonyms:
  • 5-Methyl-1,3,4-oxadiazol-2(3H)-one
  • 5-methyl-1,3,4-oxadiazol-2-ol(SALTDATA: FREE)
  • 5-Methyl-2,3-dihydro-1,3,4-oxadiazol-2-one
  • 2,3-dihydro-5-Methyl-2-oxo-1,3,4-oxadiazole
  • Methyl oxadiazolidone
  • 2-Methyl-1,3,4-Oxadiazol-5(4H)-One
  • 1,3,4-Oxadiazol-2(3H)-one, 5-methyl-
  • 5-methyl-3H,2H-1,3,4-oxadiazol-2-one
CAS:
3069-67-8
MF:
C3H4N2O2
MW:
100.08
Product Categories:
  • Heterocyclic Building Blocks
Mol File:
3069-67-8.mol
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5-Methyl-1,3,4-oxadiazol-2(3H)-one Chemical Properties

Melting point:
112 °C
Boiling point:
134 °C(Press: 14 Torr)
Density 
1.55±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
6.34±0.70(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HazardClass 
IRRITANT
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5-Methyl-1,3,4-oxadiazol-2(3H)-one Usage And Synthesis

Chemical Properties

This product is solid and insoluble in water.

Synthesis

79-20-9

1068-57-1

3069-67-8

(2) Preparation of 5-methyl-1,3,4-oxadiazolone: 2000 mL of methyl acetate was added to a 5000 mL three-necked flask and 740 g of acetylhydrazine was added slowly under stirring conditions. The reaction mixture was cooled to below 0 °C, followed by the addition of 1680 g of sodium bicarbonate in batches. The reaction unit was sealed and the phosgene was continuously vented at a flow rate of 15 m3/h. After completion of the reaction, the solvent was removed by distillation and the resulting residue was crystallized at 0 °C. The white crystals were collected by filtration to give 988.2 g of the target product in 99% yield.

References

[1] Patent: CN103724327, 2017, B. Location in patent: Paragraph 0008; 0030; 0032

5-Methyl-1,3,4-oxadiazol-2(3H)-one Preparation Products And Raw materials

Raw materials

5-Methyl-1,3,4-oxadiazol-2(3H)-oneSupplier

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