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Structure of 851435-28-4
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2-Chloro-6-methyl-N-(5-methyl-1H-pyrazol-3-yl)pyrimidin-4-amine features a pyrimidine core functionalized with a chloro group at C2, a methyl substituent at C6, and a 5-methyl-1H-pyrazol-3-yl amine at N4. This electron-deficient heterocycle integrates readily into kinase inhibitor scaffolds, offering enhanced metabolic stability and targeted binding affinity in medicinal chemistry applications.
2-Chloro-6-methyl-N-(5-methyl-1H-pyrazol-3-yl)pyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the pyrazole and methyl functionalities offer orthogonal reactivity and enhanced metabolic stability. The compound exhibits good bench stability and is compatible with standard coupling protocols, simplifying purification and scale-up in API 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: