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Structure of 116070-31-6
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2,6-Dichloro-4-methylbenzaldehyde features a sterically hindered aromatic core with electron-withdrawing chlorine atoms at the 2 and 6 positions, enhancing stability and directing electrophilic substitution. The para-methyl group provides steric and electronic modulation, while the aldehyde functionality enables direct coupling in cross-coupling reactions and condensation chemistry under standard conditions.
2,6-Dichloro-4-methylbenzaldehyde serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering enhanced electrophilicity at the carbonyl group due to electron-withdrawing chlorine substituents. Its ortho-chloro substitution provides steric protection and improves bench stability, while the methyl group enables further functionalization via oxidation or directed metallation. The compound facilitates efficient construction of substituted benzimidazoles, heterocyclic scaffolds, and arylated intermediates under standard coupling 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: