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Structure of 1194-64-5
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2-Chloro-6-methylbenzaldehyde features a chlorinated aromatic ring with a methyl group at the para position relative to the aldehyde. This electron-deficient benzaldehyde integrates readily into Suzuki and Ullmann coupling reactions, offering enhanced reactivity under standard conditions. The ortho-chloro substituent imparts steric and electronic control, enabling selective functionalization in complex synthesis.
2-Chloro-6-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the aromatic ring due to its ortho-chloro and methyl substituents. The aldehyde group facilitates efficient imine formation, reductive amination, and coupling reactions, while the chloro and methyl groups offer predictable electronic and steric modulation. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for multi-step synthesis and process development.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: