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Structure of 887573-44-6
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1-(4,6-Dichloropyridin-3-yl)ethan-1-one features a dichloropyridine core paired with a ketone functionality, enabling direct integration into heterocyclic synthesis. This bench-stable electrophile facilitates efficient coupling reactions under standard conditions, offering reliable access to functionalized pyridine derivatives for medicinal chemistry and materials applications.
1-(4,6-Dichloropyridin-3-yl)ethan-1-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds through nucleophilic substitution and coupling reactions. Its dichloro substitution pattern enhances electrophilicity at the C3 position, facilitating selective functionalization. The ketone group provides a handle for downstream transformations, including enolization and reduction, while the molecule exhibits good bench stability and compatibility with standard purification methods.
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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: