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Structure of 159326-68-8
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Pyrrolo[1,2-f][1,2,4]triazin-4-amine integrates a fused heterocyclic core with a primary amine handle, enabling direct functionalization in synthetic sequences. This electron-deficient scaffold supports efficient coupling reactions and exhibits favorable solubility in polar solvents, facilitating use in medicinal chemistry campaigns and combinatorial library synthesis.
Pyrrolo[1,2-f][1,2,4]triazin-4-amine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. Its fused tricyclic core exhibits enhanced metabolic stability and favorable π-stacking interactions, enabling efficient incorporation into kinase inhibitors and other bioactive scaffolds. The primary amine group facilitates direct derivatization via amidation, alkylation, or coupling reactions, while the electron-deficient triazine ring supports palladium-catalyzed cross-coupling. Bench-stable and readily purified by column chromatography, it functions effectively in both small-molecule discovery and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: