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Structure of 1824286-23-8
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5-Chloro-7-methoxypyrazolo[1,5-a]pyrimidine features a fused heterocyclic core with complementary electron-withdrawing and donor substituents, enabling selective coupling in late-stage functionalization. The chloro group at C5 facilitates palladium-catalyzed cross-coupling, while the methoxy moiety enhances solubility and modulates electronic properties. This scaffold serves as a key building block for kinase inhibitors and bioactive small molecules.
5-Chloro-7-methoxypyrazolo[1,5-a]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. Its chloro group facilitates nucleophilic substitution under mild conditions, while the methoxy functionality enhances solubility and modulates electronic properties. The scaffold exhibits excellent bench stability and compatibility with diverse functional groups, making it ideal for iterative synthesis campaigns targeting 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: