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Structure of 1033203-31-4
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4-Chloro-5-methylpyridin-2-amine features a pyridine core functionalized with chlorine and methyl groups at the 4- and 5-positions, respectively, enabling tailored reactivity in cross-coupling and medicinal chemistry applications. The ortho-chloro substituent enhances electrophilic engagement, while the para-methyl group provides steric and electronic modulation. This scaffold serves as a key building block for kinase inhibitors and agrochemicals, offering robust stability under standard conditions.
4-Chloro-5-methylpyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based heterocycles via palladium-catalyzed cross-coupling reactions. Its chloro group facilitates Suzuki, Stille, and Buchwald–Hartwig couplings, while the pendant amine and methyl substituents provide orthogonal reactivity for further functionalization. The compound exhibits good bench stability and ease of purification, making it well-suited for iterative synthesis workflows in API 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-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: