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Structure of 633328-98-0
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5-Chloro-1H-pyrazolo[4,3-d]pyrimidine is a heterocyclic scaffold featuring a chlorine atom at the 5-position, enabling direct functionalization in medicinal chemistry. This electron-deficient core integrates readily into kinase inhibitors and antiviral agents, offering high reactivity under standard coupling conditions. The pyrazolopyrimidine framework provides structural rigidity and enhanced binding affinity in target-directed synthesis.
5-Chloro-1H-pyrazolo[4,3-d]pyrimidine serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical synthesis. Its chloro substituent enables palladium-catalyzed cross-coupling reactions, facilitating the construction of diverse biaryl and aryl-substituted scaffolds. The core pyrazolopyrimidine framework exhibits excellent bench stability and compatibility with common functional groups, enabling efficient incorporation into complex molecular architectures through standard synthetic protocols.
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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: