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