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Structure of 63071-13-6
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4-Chloro-2-pyridinecarbaldehyde features a chlorine-substituted pyridine ring fused with an aldehyde group, enabling direct incorporation into heterocyclic scaffolds. This electron-deficient heteroaryl aldehyde serves as a key building block in medicinal chemistry and catalyst design, offering enhanced reactivity in nucleophilic addition and condensation reactions under standard conditions.
4-Chloro-2-pyridinecarbaldehyde serves as a versatile building block in medicinal chemistry and catalysis, enabling efficient construction of pyridine-based heterocycles. Its electrophilic aldehyde group facilitates nucleophilic addition reactions, while the chloropyridine moiety supports palladium-catalyzed cross-coupling transformations. The compound exhibits excellent bench stability and compatibility with common protecting groups, facilitating straightforward purification and integration into 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-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: