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Structure of 1245506-61-9
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2-Chloro-5-methoxy-4-methylpyrimidine is a bench-stable, electron-deficient pyrimidine derivative featuring orthogonal functional groups enabling selective derivatization. The chloro substituent at C2 facilitates nucleophilic substitution, while the methoxy and methyl groups at C5 and C4, respectively, provide steric and electronic modulation. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and agrochemical scaffolds.
2-Chloro-5-methoxy-4-methylpyrimidine serves as a versatile pyrimidine scaffold for medicinal chemistry and agrochemical synthesis, enabling efficient functionalization via nucleophilic substitution at the C2 position. Its methoxy and methyl groups provide orthogonal reactivity and enhanced solubility, while the chlorine facilitates coupling with amines, thiols, and heterocycles under mild conditions. Bench-stable and readily purified by column chromatography, it functions as a key building block in the construction of bioactive heterocyclic frameworks.
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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: