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Structure of 6320-15-6
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4-Chloro-2,6-dimethoxypyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring two methoxy groups that enhance solubility and modulate electronic properties. The chlorine substituent enables efficient coupling reactions, facilitating the synthesis of advanced pharmaceutical intermediates under standard conditions.
4-Chloro-2,6-dimethoxypyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions under mild conditions, while the dimethoxy substituents enhance solubility and provide orthogonal reactivity. The compound exhibits excellent bench stability and is compatible with standard coupling protocols, making it ideal 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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: