[1,2,4]Triazolo[1,5-a]pyrazine is a heterocyclic compound characterized by a fused ring system that includes both triazole and pyrazine moieties. This compound features a five-membered triazole ring and a six-membered pyrazine ring, contributing to its unique chemical properties. It is typically a crystalline solid, exhibiting moderate solubility in polar organic solvents. The presence of nitrogen atoms in its structure imparts distinct electronic properties, making it a subject of interest in various fields, including medicinal chemistry and materials science. [1,2,4]Triazolo[1,5-a]pyrazine can participate in various chemical reactions, such as nucleophilic substitutions and cycloadditions, due to its reactive nitrogen atoms. Additionally, it has been studied for its potential biological activities, including antimicrobial and anticancer properties. The compound's stability and reactivity can be influenced by substituents on the rings, allowing for the design of derivatives with tailored properties for specific applications. Overall, [1,2,4]triazolo[1,5-a]pyrazine is a versatile compound with significant implications in research and development.

[1,2,4]triazolo[1,5-a]pyrazine

399-66-6: [1,2,4]Triazolo[1,5-a]pyrazine is a heterocyclic compound characterized by a fused ring system that includes both triazole and pyrazine moieties. This compound features a five-membered triazole ring and a six-membered pyrazine ring, contributing to its unique chemical properties. It is typically a crystalline solid, exhibiting moderate solubility in polar organic solvents. The presence of nitrogen atoms in its structure imparts distinct electronic properties, making it a subject of interest in various fields, including medicinal chemistry and materials science. [1,2,4]Triazolo[1,5-a]pyrazine can participate in various chemical reactions, such as nucleophilic substitutions and cycloadditions, due to its reactive nitrogen atoms. Additionally, it has been studied for its potential biological activities, including antimicrobial and anticancer properties. The compound's stability and reactivity can be influenced by substituents on the rings, allowing for the design of derivatives with tailored properties for specific applications. Overall, [1,2,4]triazolo[1,5-a]pyrazine is a versatile compound with significant implications in research and development.

CAS 399-66-6

[1,2,4]triazolo[1,5-a]pyrazine

[1,2,4]Triazolo[1,5-a]pyrazine

Ref: IN-DA0076EN

[1,2,4]Triazolo[1,5-a]pyrazine

Ref: 54-OR91306

[1,2,4]Triazolo[1,5-a]pyrazine

Ref: 10-F319450