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Structure of 91322-00-8
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2,4,6-Trichloropyrimidin-5-amine features three chlorine substituents at key positions on the pyrimidine ring, enabling robust coupling reactions in synthetic chemistry. This electron-deficient heterocycle serves as a pivotal scaffold for constructing pharmaceutical intermediates and functional materials. The amine group facilitates nucleophilic substitution, while the trichloro pattern enhances reactivity under mild conditions. Bench-stable and moisture-tolerant, it streamlines access to complex architectures in medicinal chemistry and agrochemical development.
2,4,6-Trichloropyrimidin-5-amine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds. Its three chlorine substituents provide orthogonal reactivity for nucleophilic substitution, facilitating the introduction of diverse amine, thiol, or ether functionalities. The compound exhibits excellent bench stability and is compatible with standard reaction conditions, making it a practical choice for modular synthesis 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#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: