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Structure of 54439-75-7
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2-Chloro-4-methoxybenzaldehyde features a chlorine atom at the ortho position and a methoxy group at the para position relative to the aldehyde, creating a polarized electron-deficient aromatic system. This configuration enhances reactivity in nucleophilic addition and coupling reactions. The compound exhibits bench-stable handling characteristics under standard conditions and integrates readily into synthetic pathways requiring directed functionalization.
2-Chloro-4-methoxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of biologically active heterocycles. Its ortho-chloro and para-methoxy substituents provide enhanced reactivity in nucleophilic aromatic substitution and coupling reactions, while the aldehyde functionality facilitates imine formation and Ugi-type multicomponent reactions. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows requiring functional group compatibility and predictable regioselectivity.
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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: