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Structure of 89466-42-2
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4-Chloro-6-methoxy-2-(methylthio)pyrimidine features a trifunctional pyrimidine core enabling direct integration into heterocyclic scaffolds. The chloro group serves as a reactive handle for nucleophilic substitution, while the methoxy and methylthio substituents modulate electronic distribution and solubility. This compound demonstrates bench-stable handling under standard conditions and is well-suited for synthetic elaboration in medicinal chemistry campaigns.
4-Chloro-6-methoxy-2-(methylthio)pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the methoxy and methylthio functionalities offer orthogonal reactivity for downstream functionalization. Its bench-stable nature and compatibility with common coupling conditions make it well-suited for medicinal chemistry campaigns 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#: 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: