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Structure of 4316-93-2
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4,6-Dichloro-5-nitropyrimidine is a highly reactive heterocyclic building block featuring two chlorine substituents and a nitro group positioned for selective functionalization. This electron-deficient scaffold enables efficient coupling reactions in medicinal chemistry and agrochemical synthesis. The molecule exhibits excellent stability under standard conditions, facilitating straightforward incorporation into complex molecular architectures.
4,6-Dichloro-5-nitropyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds through orthogonal functionalization. The dichloro substitution pattern facilitates selective nucleophilic aromatic substitution under mild conditions, while the nitro group provides a handle for reduction and subsequent derivatization. Its bench-stable nature and compatibility with common reaction protocols make it well-suited for medicinal chemistry and process development workflows.
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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#: 3335
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Class : 9
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Packing Group : Ⅲ
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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: