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Structure of 14394-56-0
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6-Chloro-5-methylpyrimidin-4-amine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorine atom at C6 and a methyl group at C5, which modulates electronic properties and metabolic stability. The primary amine at C4 enables direct coupling in synthetic transformations, facilitating rapid access to diverse pyrimidine-based compounds for drug discovery applications.
6-Chloro-5-methylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. Its chloro and amino groups offer orthogonal reactivity for cross-coupling, nucleophilic substitution, and cyclization reactions. The methyl group enhances lipophilicity and metabolic stability, while the compound exhibits excellent bench stability and ease of purification—ideal for iterative synthesis in API development and heterocycle construction 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: