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Structure of 58966-34-0
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5-Chloro-2-methylbenzaldehyde features a chlorinated aromatic ring with ortho-methyl and aldehyde functionalities, enabling direct integration into Suzuki-Miyaura couplings and aldol condensations. This electron-deficient aldehyde offers enhanced reactivity in C–C bond formation under mild conditions, delivering high yields in pharmaceutical intermediates and functionalized heterocycles.
5-Chloro-2-methylbenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted aromatic scaffolds. Its ortho-methyl and meta-chloro substituents provide directed functionalization opportunities and enhance metabolic stability in bioactive molecule design. The aldehyde group facilitates nucleophilic addition, condensation, and coupling reactions under mild conditions, offering reliable reactivity with broad functional group tolerance. Bench-stable and readily purified by distillation or recrystallization, it functions effectively in multistep synthesis, including the construction of heterocyclic intermediates and pharmaceutical candidates.
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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: