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Structure of 90064-48-5
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4-Chloro-2,5-dimethoxybenzaldehyde features a chlorine-substituted aromatic ring flanked by two methoxy groups and a formyl moiety, enabling direct incorporation into diverse heterocyclic scaffolds. This electron-deficient aldehyde facilitates efficient coupling reactions under standard conditions, offering high functional group tolerance and stability during synthetic manipulations.
4-Chloro-2,5-dimethoxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted aromatic scaffolds. Its aldehyde functionality facilitates reductive amination, Grignard additions, and Ullmann-type coupling reactions. The ortho-dimethoxy substitution pattern enhances regioselectivity in electrophilic functionalization, while the 4-chloro group provides a handle for palladium-catalyzed cross-coupling transformations. Bench-stable and readily purified by crystallization, it supports scalable synthesis workflows.
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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: