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Structure of 91591-70-7
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2,6-Dichloro-4-methylnicotinaldehyde is a bench-stable, electron-deficient aldehyde featuring two chlorine substituents at the 2 and 6 positions of the pyridine ring, which enhances reactivity in nucleophilic additions. The para-methyl group at the 4-position imparts steric and electronic modulation, enabling selective coupling reactions in synthetic medicinal chemistry and heterocyclic scaffold construction.
2,6-Dichloro-4-methylnicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds via standard condensation and coupling reactions. Its electron-deficient aromatic core enhances reactivity in nucleophilic additions and facilitates regioselective functionalization. The dichloro substitution pattern provides orthogonal handles for further derivatization, while the aldehyde group allows direct incorporation into imine-based transformations. Bench-stable and readily purified by distillation or chromatography, it functions effectively in multistep syntheses of bioactive heterocycles and pharmaceutical intermediates.
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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
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Precautionary Statements : P261-P280-P304+P340-P405
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Lot numbers can be found on the outside label of a product: