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*For research and further manufacturing use only, not for direct human use.
Structure of 1604-14-4
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Ethyl 2,6-dichloroisonicotinate features a pyridine core with strategically positioned chlorine substituents at the 2- and 6-positions, enhancing electrophilic reactivity. This electron-deficient heterocycle integrates readily into synthetic sequences requiring halogen-directed functionalization. The ethyl ester group enables direct manipulation via hydrolysis or nucleophilic substitution. Bench-stable and moisture-tolerant, it serves as a robust building block for pharmaceutical intermediates and agrochemicals.
Ethyl 2,6-dichloroisonicotinate serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted isonicotinates and heterocyclic scaffolds. Its dual chloro substituents enhance electrophilicity at the ring, facilitating nucleophilic aromatic substitution and transition-metal-catalyzed coupling reactions. The ester group provides a handle for selective transformations, while the compound exhibits good bench stability and ease of purification—key attributes for scalable synthesis and process 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: