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Structure of 26218-75-7
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Methyl 6-bromopicolinate features a brominated pyridine ring with a methyl ester handle, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This bench-stable derivative integrates readily into complex heterocyclic scaffolds under standard conditions.
Methyl 6-bromopicolinate serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the C-6 position via palladium-catalyzed cross-coupling reactions. Its bromine substituent exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the ester group provides orthogonal handle for further transformations. The compound demonstrates excellent bench stability and facilitates efficient purification, making it well-suited for iterative synthesis of heterocyclic scaffolds and pharmaceutical intermediates.
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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 : H315-H319
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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: