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Structure of 2825693-21-6
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2,4-Dichloropyrazolo[1,5-a][1,3,5]triazine features a rigid, electron-deficient heterocyclic core that enables direct functionalization at the pyrazole and triazine positions. This scaffold integrates readily into synthetic routes requiring high thermal stability and predictable reactivity, particularly in medicinal chemistry and agrochemical development.
2,4-Dichloropyrazolo[1,5-a][1,3,5]triazine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through palladium-catalyzed cross-coupling reactions. Its dichloro substitution pattern facilitates selective functionalization at C2 and C4 positions, offering excellent stability under standard reaction conditions. The compound exhibits high compatibility with diverse nucleophiles, including amines and thiols, and is readily purified by crystallization or flash chromatography—making it ideal for scalable synthesis of kinase inhibitors and other bioactive molecules.
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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 : H317
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Precautionary Statements : P261-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: