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Structure of 1780378-34-8
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2-Bromo-5-chloropyrazolo[1,5-a]pyrimidine features a fused heterocyclic core with complementary halogen substituents enabling direct functionalization in cross-coupling reactions. The electron-deficient pyrazolopyrimidine scaffold supports efficient derivatization under palladium catalysis, delivering complex molecular architectures for medicinal chemistry and materials science applications.
2-Bromo-5-chloropyrazolo[1,5-a]pyrimidine serves as a versatile building block for constructing substituted heterocycles in medicinal chemistry and agrochemical research. Its dual halogenation enables efficient Pd-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig aminations, with excellent functional group tolerance. The molecule exhibits good bench stability and facilitates rapid diversification of pyrazolo[1,5-a]pyrimidine scaffolds under standard reaction conditions.
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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: