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Structure of 114077-82-6
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4-Chloropyridine-3-carbaldehyde features a pyridine ring bearing both chloro and aldehyde functionalities, enabling direct incorporation into heterocyclic synthesis. The electron-deficient aldehyde group facilitates nucleophilic additions, while the para-chloro substituent supports palladium-catalyzed coupling reactions. This bifunctional scaffold delivers efficient access to bioactive molecules in medicinal chemistry.
4-Chloropyridine-3-carbaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds through nucleophilic addition and coupling reactions. Its orthogonal reactivity profile—combining an electrophilic aldehyde with a halogen-bearing pyridine ring—facilitates sequential functionalization in medicinal chemistry and agrochemical development. The compound exhibits excellent bench stability and is compatible with standard purification methods, supporting scalable 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: