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Structure of 3029-64-9
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2,4,6-Trichloro-5-cyanopyrimidine features a highly electron-deficient pyrimidine core with three chloro groups and a cyano substituent, enabling efficient coupling in nucleophilic substitution reactions. This reactivity profile supports direct functionalization of heterocycles under mild conditions. The compound exhibits robust stability during storage and handling, making it well-suited for synthetic applications requiring precise regiocontrol.
2,4,6-Trichloro-5-cyanopyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via nucleophilic aromatic substitution. Its three chlorine atoms exhibit high reactivity toward diverse nucleophiles, while the cyano group provides a handle for further functionalization. The compound demonstrates excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and agrochemical development.
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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: