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Structure of 5305-45-3
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4,6-Dichloropyrimidine-5-carbonitrile features a highly reactive pyrimidine core with dual chlorine sites and a nitrile group, enabling selective functionalization in medicinal chemistry. This electron-deficient heterocycle integrates readily into complex scaffolds under mild conditions, offering efficient access to bioactive molecules through cross-coupling and nucleophilic substitution reactions.
4,6-Dichloropyrimidine-5-carbonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its dual chloro groups enable selective nucleophilic substitution, while the nitrile moiety provides a handle for downstream transformations. The compound exhibits good bench stability and facilitates efficient construction of pyrimidine-based scaffolds via coupling reactions, making it valuable for developing functionalized heterocycles in high-throughput screening campaigns.
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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: