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Structure of 113293-70-2
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2,6-Dichloroisonicotinaldehyde features a sterically hindered pyridine core with electron-withdrawing chlorine substituents at the 2 and 6 positions, enhancing its electrophilicity. This configuration promotes efficient coupling in cross-coupling reactions and improves stability under standard handling conditions. The aldehyde functionality enables direct incorporation into heterocyclic scaffolds and conjugated systems.
2,6-Dichloroisonicotinaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of heterocyclic scaffolds and functionalized aromatic systems. Its dual chloro substituents enhance electrophilicity at the aldehyde carbon, facilitating nucleophilic addition and condensation reactions. The molecule exhibits good bench stability and is compatible with standard purification methods, making it suitable for use in medicinal chemistry campaigns and process development 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: