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Structure of 60703-46-0
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2,4,6-Trichloro-5-methoxypyrimidine serves as a pivotal electrophilic scaffold in heterocyclic synthesis. The methoxy group at the 5-position enhances solubility and directs regioselective functionalization. This bench-stable pyrimidine derivative facilitates efficient coupling reactions under mild conditions, enabling rapid access to complex nitrogen-containing architectures.
2,4,6-Trichloro-5-methoxypyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its three chlorines provide orthogonal reactivity for sequential nucleophilic substitutions, facilitating the installation of diverse aryl, alkyl, and amine functionalities under mild conditions. The methoxy group enhances solubility and stability, supporting reliable handling and purification. Widely used in medicinal chemistry and agrochemical development, it functions as a key intermediate for functionalized pyrimidines with proven utility in drug discovery 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 : 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: