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Structure of 884495-36-7
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6-Chloro-2-methylnicotinaldehyde features a chlorine-substituted pyridine ring with a methylene group at the 2-position and an aldehyde functionality at the 6-position. This electron-deficient heterocyclic scaffold integrates readily into synthetic routes for bioactive molecules, offering enhanced reactivity in coupling and condensation reactions under standard conditions.
6-Chloro-2-methylnicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted pyridine and nicotinamide derivatives. Its aldehyde functionality facilitates reductive amination, condensation, and coupling reactions, while the 6-chloro and 2-methyl substituents provide orthogonal reactivity and steric modulation. The compound exhibits good bench stability and is compatible with standard purification protocols, making it suitable for scale-up and multi-step 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: