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Structure of 947179-03-5
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Ethyl 4-bromo-6-methylpicolinate features a brominated pyridine core with strategic methyl and ester functionalities, enabling direct incorporation into cross-coupling reactions. The para-bromine serves as a reliable handle for palladium-mediated transformations, while the electron-deficient ring enhances reactivity in nucleophilic substitution processes. This bench-stable intermediate supports efficient synthesis of bioactive heterocycles and pharmaceutical scaffolds under standard conditions.
Ethyl 4-bromo-6-methylpicolinate serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-established bromine functionality. The ester group facilitates further transformations, while the methyl and picolinate moieties provide structural rigidity and polarity suitable for targeted heterocycle synthesis. Bench-stable and amenable to standard purification methods, it functions reliably in multi-step synthetic sequences.
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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: