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Structure of 154012-15-4
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Ethyl 4,6-dichloro-5-nitronicotinate features a dual chloro substitution at the 4- and 6-positions flanking a nitro group at C5 on a nicotinate core. This electron-deficient heterocycle serves as a pivotal building block in medicinal chemistry, enabling direct incorporation into complex scaffolds via cross-coupling or nucleophilic displacement reactions under standard conditions.
Ethyl 4,6-dichloro-5-nitronicotinate serves as a versatile building block in heterocyclic synthesis, enabling the construction of substituted pyridine scaffolds via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The dichloro and nitro groups provide orthogonal reactivity for sequential functionalization, while the ethyl ester facilitates downstream transformations. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for medicinal chemistry and process development 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: