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Structure of 72232-49-6
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2-Chloro-3-methoxyphenol features a chlorinated aromatic ring paired with a methoxy substituent, delivering enhanced electron density at the ortho position. This combination enables selective functionalization in synthetic pathways and supports stability under standard bench conditions. The molecule integrates readily into complex phenolic scaffolds used in pharmaceutical intermediates and agrochemical development.
2-Chloro-3-methoxyphenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted aromatic scaffolds. Its ortho-chloro and meta-methoxy functionalities provide orthogonal reactivity for palladium-catalyzed cross-couplings and electrophilic substitutions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic sequences 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: