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Structure of 932-32-1
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2-Chloro-N-methylaniline features a chlorinated aromatic ring paired with a methylaniline functionality, delivering enhanced reactivity in electrophilic substitution and improved solubility over unsubstituted aniline analogs. This bench-stable compound integrates readily into pharmaceutical intermediates and specialty dye synthesis.
2-Chloro-N-methylaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the aromatic ring due to its activated chlorine substituent. The N-methyl group enhances solubility and modulates electronic properties, while the compound exhibits excellent bench stability and compatibility with standard coupling reactions. It functions as a key intermediate in constructing heterocyclic scaffolds and bioactive molecules via palladium-catalyzed cross-coupling or nucleophilic substitution.
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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 : H315-H319-H335
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Precautionary Statements : P261-P305+P351+P338
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Lot numbers can be found on the outside label of a product: