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Structure of 36340-61-1
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2-Amino-4-chloro-6-methylpyridine features a pyridine core functionalized with an amino group at position 2, a chlorine atom at position 4, and a methyl substituent at position 6. This electron-deficient heterocycle serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, offering enhanced reactivity in cross-coupling and nucleophilic substitution processes under standard conditions.
2-Amino-4-chloro-6-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted pyridine scaffolds. Its amino and chloro groups provide orthogonal reactivity for Suzuki-Miyaura couplings, nucleophilic substitutions, and metal-catalyzed cross-coupling transformations. The methyl group enhances metabolic stability and modulates electronic properties, while the compound exhibits excellent bench stability and ease of purification, making it well-suited for scalable laboratory applications.
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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: