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Structure of 874-27-1
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3-Chloro-2-methylbenzaldehyde features a chlorinated aromatic ring with adjacent methyl and aldehyde groups, delivering enhanced reactivity in electrophilic substitution. This ortho-substituted scaffold enables efficient integration into pharmaceutical intermediates and functional materials. The molecule exhibits favorable stability under standard bench conditions, facilitating straightforward handling in synthetic workflows.
3-Chloro-2-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, benzoxazoles, and other heterocyclic scaffolds via standard condensation and cyclization protocols. Its ortho-chloro and methyl substituents provide controlled reactivity and steric modulation, enhancing regioselectivity in electrophilic aromatic substitution and coupling reactions. Bench-stable and readily purified by distillation or recrystallization, it functions effectively in multi-step syntheses requiring functional group tolerance and predictable transformation pathways.
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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: