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Structure of 779353-64-9
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5,7-Dichloro-3-ethylpyrazolo[1,5-a]pyrimidine features a rigid heteroaromatic core with strategically positioned electron-withdrawing chloro groups and a lipophilic ethyl substituent. This combination enhances its utility in constructing bioactive scaffolds, particularly in kinase inhibitor development and medicinal chemistry campaigns requiring moderate metabolic stability and controlled reactivity under standard conditions.
5,7-Dichloro-3-ethylpyrazolo[1,5-a]pyrimidine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of kinase inhibitor scaffolds. Its electron-deficient pyrazolopyrimidine core facilitates nucleophilic substitution and palladium-catalyzed coupling reactions. The dichloro substituents provide orthogonal reactivity for selective functionalization, while the ethyl group enhances solubility and modulates electronic properties. Bench-stable and amenable to standard purification methods, it functions reliably in multi-step syntheses targeting 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 : 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: