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Structure of 940284-55-9
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Ethyl 5,7-dichloropyrazolo[1,5-a]pyrimidine-3-carboxylate features a rigid heterocyclic core bearing two chlorine substituents at electron-deficient positions, enabling efficient coupling in cross-coupling reactions. This bench-stable derivative integrates readily into complex molecular architectures under standard conditions, offering high functional group tolerance and predictable reactivity in medicinal chemistry and materials synthesis workflows.
Ethyl 5,7-dichloropyrazolo[1,5-a]pyrimidine-3-carboxylate serves as a versatile building block for the synthesis of substituted pyrazolo[1,5-a]pyrimidines, key scaffolds in medicinal chemistry. The molecule features two chlorine atoms at positions 5 and 7, enabling directed functionalization via nucleophilic substitution. Its ethyl ester group facilitates downstream transformations such as hydrolysis or coupling reactions. The compound exhibits good bench stability and is compatible with standard reaction conditions, making it well-suited for iterative synthetic workflows in API development and heterocyclic library generation.
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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-H312-H315-H319-H332-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: