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Structure of 615-65-6
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2-Chloro-4-methylaniline features a chlorinated aromatic ring paired with an electron-donating methyl group, enabling selective coupling reactions in pharmaceutical intermediates. This bench-stable derivative integrates efficiently into heterocyclic scaffolds under standard conditions.
2-Chloro-4-methylaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct incorporation of both chloro and methyl substituents on an aniline scaffold. Its reactivity facilitates electrophilic substitution, palladium-catalyzed coupling reactions, and amide formation under standard conditions. The compound exhibits good bench stability and is readily purified by recrystallization or column chromatography, making it suitable for scalable synthesis workflows.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3429
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302+H312+H332-H315-H318-H412
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: