N-(6-methyl-3-oxo-2,5-dihydro-1,2,4-triazin-4-yl)acetamide
N-(6-Methyl-3-oxo-2,5-dihydro-1,2,4-triazin-4(3H)-yl)acetamide
CAS: 136738-23-3
Molecular Formula: C6H10N4O2
N-(6-methyl-3-oxo-2,5-dihydro-1,2,4-triazin-4-yl)acetamide - Names and Identifiers
N-(6-methyl-3-oxo-2,5-dihydro-1,2,4-triazin-4-yl)acetamide - Physico-chemical Properties
| Molecular Formula | C6H10N4O2 |
| Molar Mass | 170.17 |
| Density | 1.43±0.1 g/cm3(Predicted) |
| pKa | 11.22±0.40(Predicted) |
| Storage Condition | 2-8 ℃, dry, sealed |
N-(6-methyl-3-oxo-2,5-dihydro-1,2,4-triazin-4-yl)acetamide - Introduction
Triazine amide is an organic compound with the chemical formula C3H3N7O. It has the following properties:
1. physical properties: triazine amide is colorless crystal or white crystalline powder, soluble in hot water and organic solvents, insoluble in alcohol and ether.
2. Chemical properties: Triazine amide is a stable compound with good thermal stability. It can decompose at high temperatures, giving off ammonia and nitrogen.
The main uses of triazine amide are:
1. chemical intermediates: triazine amide can be used as an intermediate for the synthesis of organic compounds. It is widely used in drug synthesis, pigment synthesis, medicine, pesticide and dye industry.
2. Provide nitrogen source: triazine amide can be added to the matrix as a nitrogen source to promote the growth of plants.
preparation of triazine amide methods generally have the following:
1. ammonia cyanic acid and urea reaction: ammonia cyanic acid and urea in acid or alkali catalysis, the formation of triazine amide.
2. pyrolysis urea amine: urea amine is subjected to pyrolysis reaction at high temperature to obtain triazine amide.
3. phosgene method: reaction of urea amine and phosgene to generate triazine amide.
Regarding the safety information of triazine amide, the following points should be noted:
1. toxicity: triazine amide on the human body has a certain irritation, may cause damage to the respiratory tract, eyes and skin. Avoid contact with skin, eyes, and respiratory tract during use or handling.
2. fire hazard: triazine amide may produce toxic gases and corrosive substances at high temperatures, and there is a risk of fire. Keep away from open flames, heat sources and oxidants.
3. Storage Note: Triazine amide should be stored in a cool, dry, well-ventilated place to avoid contact with oxidants and combustibles.
1. physical properties: triazine amide is colorless crystal or white crystalline powder, soluble in hot water and organic solvents, insoluble in alcohol and ether.
2. Chemical properties: Triazine amide is a stable compound with good thermal stability. It can decompose at high temperatures, giving off ammonia and nitrogen.
The main uses of triazine amide are:
1. chemical intermediates: triazine amide can be used as an intermediate for the synthesis of organic compounds. It is widely used in drug synthesis, pigment synthesis, medicine, pesticide and dye industry.
2. Provide nitrogen source: triazine amide can be added to the matrix as a nitrogen source to promote the growth of plants.
preparation of triazine amide methods generally have the following:
1. ammonia cyanic acid and urea reaction: ammonia cyanic acid and urea in acid or alkali catalysis, the formation of triazine amide.
2. pyrolysis urea amine: urea amine is subjected to pyrolysis reaction at high temperature to obtain triazine amide.
3. phosgene method: reaction of urea amine and phosgene to generate triazine amide.
Regarding the safety information of triazine amide, the following points should be noted:
1. toxicity: triazine amide on the human body has a certain irritation, may cause damage to the respiratory tract, eyes and skin. Avoid contact with skin, eyes, and respiratory tract during use or handling.
2. fire hazard: triazine amide may produce toxic gases and corrosive substances at high temperatures, and there is a risk of fire. Keep away from open flames, heat sources and oxidants.
3. Storage Note: Triazine amide should be stored in a cool, dry, well-ventilated place to avoid contact with oxidants and combustibles.
Last Update：2024-04-09 21:21:28
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