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Structure of 5193-88-4
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4-Chloro-5,6-dimethoxypyrimidine features a pyrimidine core functionalized with chlorine and two methoxy groups, enabling selective coupling in heterocyclic synthesis. The electron-deficient ring facilitates nucleophilic substitution, while the dimethoxy substituents enhance solubility and stability under standard conditions. This scaffold integrates efficiently into pharmaceutical intermediates and agrochemical building blocks.
4-Chloro-5,6-dimethoxypyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions with amines, thiols, and other heteroatoms, while the dimethoxy substituents enhance solubility and modulate reactivity. Its bench-stable nature and compatibility with standard coupling conditions make it ideal for parallel synthesis workflows and API intermediate development.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: