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Structure of 95652-81-6
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6-Chloro-2-methoxynicotinaldehyde features a chlorine substituent at the 6-position and a methoxy group at the 2-position, creating a highly electron-deficient pyridine core. This configuration enhances reactivity in nucleophilic addition and coupling processes, particularly in the synthesis of heterocyclic scaffolds and bioactive molecules. The aldehyde functionality enables direct integration into complex architectures under mild conditions.
6-Chloro-2-methoxynicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted pyridine scaffolds via standard coupling reactions. Its orthogonal functional groups—chlorine at C6 and methoxy at C2—facilitate selective transformations, while the aldehyde functionality supports reductive amination, imine formation, and Ugi-type condensations. The compound exhibits good bench stability and is amenable to purification by column chromatography or distillation, supporting its use in multi-step syntheses.
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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-H317-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P272-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: