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Structure of 1702-18-7
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3,6-Dichloro-2-pyridinecarbonitrile features a rigid pyridine core bearing two chlorine substituents at the 3 and 6 positions and a nitrile group at C2. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a key building block in agrochemical and pharmaceutical synthesis. The molecule exhibits enhanced stability under standard conditions and facilitates efficient functionalization via nucleophilic substitution or metal-mediated transformations.
3,6-Dichloro-2-pyridinecarbonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of functionalized pyridine scaffolds. Its dual halogen and nitrile groups facilitate palladium-catalyzed cross-coupling reactions and nucleophilic substitution pathways under mild conditions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable synthetic 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: