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Structure of 61098-37-1
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Ethyl 7-chloropyrazolo[1,5-a]pyrimidine-5-carboxylate features a chlorinated pyrazolo[1,5-a]pyrimidine core with an ethyl ester handle, enabling direct incorporation into heterocyclic scaffolds. This bench-stable, moisture-tolerant building block facilitates efficient access to bioactive compounds through palladium-catalyzed cross-coupling and nucleophilic substitution reactions.
Ethyl 7-chloropyrazolo[1,5-a]pyrimidine-5-carboxylate serves as a versatile building block for the synthesis of substituted pyrazolo[1,5-a]pyrimidines. The chloro group at the 7-position enables facile nucleophilic substitution, while the ester functionality supports further derivatization via hydrolysis or reduction. This compound exhibits excellent bench stability and functional group tolerance, facilitating its use in standard coupling reactions and heterocycle elaboration workflows common in medicinal chemistry and agrochemical research.
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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: