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Structure of 4903-09-7
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3-Chloro-4-methoxybenzaldehyde features a chlorine substituent at the meta position and a methoxy group at the para position relative to the aldehyde, delivering enhanced electron-withdrawing character and improved solubility in polar organic solvents. This configuration enables efficient coupling reactions in pharmaceutical intermediates and functional material synthesis.
3-Chloro-4-methoxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzene scaffolds. Its orthogonal functional groups—chlorine and methoxy—facilitate diverse downstream transformations including Suzuki-Miyaura coupling, nucleophilic substitution, and electrophilic aromatic substitution. The aldehyde group provides a key handle for reductive amination, imine formation, and Ugi-type condensations. Bench-stable and readily purified by recrystallization, it supports scalable synthesis with predictable regioselectivity in standard reaction conditions.
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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: