246048-63-5

Usage

Class

Oxadiazole derivative
It belongs to a class of organic compounds containing a five-membered heterocyclic ring with oxygen and two nitrogen atoms.

Structure

Methyl ester of 1,2,5-oxadiazole-3-carboximidic acid, 4-amino
The compound is derived from 1,2,5-oxadiazole-3-carboximidic acid by attaching a methyl ester group and an amino group at the 4-position.

Applications

Research and development
It is used as a building block in the synthesis of pharmaceuticals and agrochemicals.

Potential applications

Materials science
The compound may have potential applications in materials science due to its unique structure and properties.

Precursor

Preparation of other organic compounds
It can be used as a precursor for the preparation of other organic compounds with desired properties.

Solubility

Unknown (depends on the solvent)
The solubility of the compound in various solvents is not provided, but it can vary depending on the solvent used.

Stability

Unknown (depends on conditions)
The stability of the compound under different conditions (e.g., temperature, pressure, presence of other chemicals) is not provided.

Reactivity

Unknown (depends on the reaction conditions)
The reactivity of the compound with other chemicals or under specific reaction conditions is not provided.

Upstream product

• 67-56-1 methanol 
• 156463-85-3 3-amino-1,2,5-oxadiazole-4-carbonitrile 
• 124-41-4 sodium methylate 

Downstream Products

• 581081-13-2 C₁₅H₁₁N₅O 
• 581081-47-2 C₁₆H₁₃N₅O₂ 
• 581081-48-3 C₁₆H₁₃N₅O₂ 
• 908590-49-8 C₁₅H₁₇N₅O 
• 293760-29-9 3-amino-4-(1-ethyl-1H-benzo[d]imidazol-2-yl)-1,2,5-oxadiazole 
• 581081-50-7 C₁₆H₁₃N₅O₂ 
• 581081-62-1 C₁₆H₁₀N₆O 
• 581081-56-3 C₁₆H₁₀N₆O 
• 581081-52-9 C₁₆H₁₀N₆O 
• 332026-86-5 3-amino-4-(1H-benzo[d]imidazol-2-yl)-1,2,5-oxadiazole 
• 13300-88-4 4-amino-1,2,5-oxadiazole-3-carboxylic acid amide 

Relevant academic research and scientific papers

Chromone-containing benzimidazole bifurazan compound with Cy-FBP/SBPase inhibition effect and preparation method of chromone-containing benzimidazole bifurazan compound

The invention provides a chromone-containing benzimidazole bifurazan compound with a Cy-FBP/SBPase inhibition effect and a preparation method of the chromone-containing benzimidazole bifurazan compound. The molecular structure of the compound is shown as

A novel energetic framework combining the advantages of furazan and triazole: A design for high-performance insensitive explosives

A series of tetracyclic furazan-triazole compounds have been synthesized and fully characterized. The predicted detonation performance and tested mechanical sensitivities showed their high-energy performance and insensitive features. Quantum chemical calculations and crystal structure analysis were applied to study the intrinsic structure-property relationship among these compounds. In addition, the detonation test shows their promising potential as secondary explosives.

Benzimidazole bifurazan series compounds and synthesis method thereof

The invention provides benzimidazole bifurazan series compounds and a synthesis method thereof. The molecular structure of the compounds is represented by a formula I, wherein R1 is selected from hydrogen, halogen, trifluoromethyl, nitryl, amino, sulfo, methyl, tert-butyl, methoxyl, carboxyl, ethoxyformyl or benzoyl; R2 is selected from hydrogen or fluorine. On the basis, the invention discloses an efficient method for preparing the series of compounds. The preparation method comprises the steps: synthesizing an intermediate 4-amino-1,2,5-oxadiazole-3-methoxyamidine by taking malononitrile asa starting raw material, carrying out a reaction on the intermediate with o-phenylenediamine or a substitute thereof under a heating reflux condition by taking acetic acid as a solvent, cooling, adding water, stirring to separate out a solid after the reaction is finished, and carrying out suction filtration, washing, drying and the like to obtain a final product. According to the method, a pure product can be obtained without recrystallization, column chromatography separation and other steps, the method is simple, rapid and practical, and the yield can generally reach 80% or above.

Synthesis and properties of iminoester of 3-aminofurazan-4-carboxylic acid

Iminoester of 3-aminofurazan-4-carboxylic acid was synthesized for the first time. Starting with the iminoester were prepared amidrazone of 3-aminofurazan-4-carboxylic acid, 1,4-diamino-1,4-bis(3-aminofurazan-4-yl)-2,3-diaza-1,3-butadiene, 1-amino-1,4-bis(3-aminofurazan-4-yl)-4-oxo-2,3-diaza-1-butene, and 3,5-bis(3-aminofurazan-4-yl)-1H-1,2,4-triazole. The alkylation of the latter with methyl iodide gave rise to a mixture of 1- and 4-methyl-3,5-bis(3-aminofurazan-4-yl)-1,2,4-triazole containing predominantly 1-isomer.