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Structure of 615-62-3
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3-Chloro-4-methylphenol features a chlorinated aromatic ring with adjacent methyl and hydroxyl groups, delivering enhanced reactivity for electrophilic substitution. This electron-rich scaffold enables direct functionalization in synthetic pathways, particularly useful in agrochemical and pharmaceutical intermediates. The molecule exhibits bench-stable handling under standard conditions.
3-Chloro-4-methylphenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted aromatic scaffolds. Its ortho-chloro and para-methyl groups provide distinct reactivity profiles for palladium-catalyzed coupling reactions and electrophilic functionalization. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for scale-up and multi-step synthetic sequences.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302+H312+H332-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: