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Structure of 42754-96-1
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4,6-Dichloro-1H-pyrazolo[3,4-d]pyrimidine is a heterocyclic scaffold featuring two chlorine substituents at electron-deficient positions, enabling efficient coupling in transition-metal-catalyzed reactions. This bench-stable core integrates readily into kinase inhibitors and nucleoside analogs, offering high reactivity under standard conditions.
4,6-Dichloro-1H-pyrazolo[3,4-d]pyrimidine serves as a versatile building block for the synthesis of biologically active heterocycles, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its dual chloro substituents offer orthogonal reactivity, facilitating sequential derivatization while maintaining bench stability and ease of purification. Functions effectively in the construction of kinase inhibitor scaffolds and other pharmaceutical intermediates.
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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: