Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo-[1,2-f][1,2,4]triazine-6-carboxylate - Names and Identifiers
Name | Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo-[1,2-f][1,2,4]triazine-6-carboxylate
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Synonyms | Ethyl 4-hydroxy-5-Methylp... Ethyl 4-hydroxy-5-methylpyrrolo[1,2-f][1,2,4]triazine-6-carboxylate Ethyl 4-hydroxy-5-Methylpyrrolo[2,1-f][1,2,4]triazine-6-carboxylate Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo[1,2-f][1,2,4]triazine-6-carboxylate ethyl 5-Methyl-4-oxo-3,4-dihydropyrrolo[2,1-f][1,2,4]triazine-6-carboxylate Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo-[1,2-f][1,2,4]triazine-6-carboxylate ethyl 4-hydroxy-5-Methyl -4a,5-dihydro pyrrolo[1,2-f][1,2,4]triazine-6-carboxylate 5-Methyl-4-oxo-3,4-dihydro-pyrrolo[2,1-f][1,2,4]triazine-6-carboxylic acid ethyl ester Pyrrolo[2,1-f][1,2,4]triazine-6-carboxylic acid, 1,4-dihydro-5-methyl-4-oxo-, ethyl ester
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CAS | 427878-70-4
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Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo-[1,2-f][1,2,4]triazine-6-carboxylate - Physico-chemical Properties
Molecular Formula | C10H11N3O3
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Molar Mass | 221.21 |
Appearance | Powder |
Color | Yellow |
Storage Condition | Sealed in dry,Room Temperature |
Sensitive | IRRITANT |
MDL | MFCD11044884 |
Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo-[1,2-f][1,2,4]triazine-6-carboxylate - Introduction
Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo-[1,2-f][1,2,4]triazine-6-carboxylate is an organic compound with the formula C11H12N4O3.
Its properties are as follows:
-Appearance: a solid powder
-Melting point: approx. 205-210°C
-Solubility: Soluble in common organic solvents, such as ethanol, dimethyl sulfoxide and dichloromethane, insoluble in water.
Its main uses include:
-Chemical reagent: It can be used as an intermediate in organic synthesis and used to synthesize other compounds.
-Drug research: has potential anti-tumor and anti-viral activity, can be used for drug development and screening.
-Pesticide research: as a candidate compound for pesticides and fungicides, used in agricultural research.
Ethyl 5-methyl-4-oxo-3,4-dihydropyrrolo-[1,2-f][1,2,4]triazine-6-carboxylate can be prepared by the following synthetic methods:
First, N-methylpyrrolidin-2-one was synthesized by the reaction of N-methylpyrrolidone and ethyl isocyanate using acetone as a raw material. This compound is then reacted with a mercaptoamine to form a bis-amino-imine, which undergoes dehydration and amination to form 3,4-dihydropyrrolo [1,2-f][1,2,4] triazine acid. Finally, the final ethyl ester compound is formed by esterification reaction with ethanol.
Regarding safety information, this compound may be harmful. Exposure to or inhalation of its dust may cause irritation and allergic reactions. Appropriate personal protective equipment, such as gloves and protective glasses, should be worn during handling. It should be operated in a well-ventilated area and avoid direct contact with skin and eyes. In case of accidental exposure or discomfort, medical help should be sought immediately.
Last Update:2024-04-09 21:01:54