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Structure of 24473-00-5
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2,4,6-Trichlorobenzaldehyde features a highly electron-deficient aromatic ring stabilized by three chlorine substituents, enabling efficient electrophilic coupling reactions. This bench-stable aldehyde integrates readily into synthetic sequences requiring strong inductive withdrawal, particularly in pharmaceutical intermediates and heterocyclic scaffold construction.
2,4,6-Trichlorobenzaldehyde serves as a highly functionalized aromatic aldehyde enabling efficient access to substituted heterocycles and pharmaceutical intermediates. Its electron-deficient aryl ring enhances reactivity in nucleophilic addition and condensation reactions, while the three chlorine substituents provide orthogonal handles for further derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in standard synthetic workflows including Ugi, Mannich, and Stetter reactions.
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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: