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Structure of 1093880-37-5
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6-Chloro-2-fluoronicotinaldehyde features a highly reactive aldehyde group flanked by electron-withdrawing chlorine and fluorine substituents, enhancing electrophilicity for nucleophilic addition. This bench-stable heterocyclic scaffold integrates readily into synthetic routes requiring polarized carbonyl functionality, particularly in medicinal chemistry and agrochemical development.
6-Chloro-2-fluoronicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of fluorinated heterocycles and bioactive scaffolds. Its ortho-fluoro and meta-chloro substituents enhance electrophilicity at the aldehyde position, facilitating efficient nucleophilic additions and condensation reactions. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthetic workflows in API development.
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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: