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Structure of 1234616-50-2
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5-Chloropyrazolo[1,5-a]pyrimidin-3-amine features a fused heterocyclic core with a chloro substituent at the 5-position and an amine group at the 3-position. This arrangement imparts enhanced electronic density and directional reactivity, enabling efficient coupling in medicinal chemistry applications. The scaffold exhibits robust stability under standard conditions, facilitating incorporation into diverse molecular architectures for targeted drug discovery.
5-Chloropyrazolo[1,5-a]pyrimidin-3-amine serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical research. Its chloro group enables palladium-catalyzed cross-coupling reactions, while the primary amine facilitates derivatization via acylation, alkylation, or amidation. The scaffold exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for modular synthesis of functionalized pyrazolopyrimidine derivatives.
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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
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Precautionary Statements : P261-P280-P304+P340
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Lot numbers can be found on the outside label of a product: