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Structure of 1235036-15-3
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tert-Butyl 3-bromo-6-chloropicolinate features a sterically hindered tert-butyl ester paired with strategically positioned bromo and chloro substituents on the picolinate core. This combination enables direct functionalization in cross-coupling processes, where the electron-deficient pyridine ring facilitates palladium-catalyzed transformations. The molecule exhibits bench-stable handling characteristics and integrates readily into synthetic routes targeting complex heterocyclic architectures.
tert-Butyl 3-bromo-6-chloropicolinate serves as a versatile building block in medicinal chemistry and process development, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The ortho-halogenated pyridine core provides excellent regioselectivity for Suzuki, Stille, and Negishi couplings, while the tert-butyl ester offers bench stability and straightforward deprotection under mild acidic conditions. Its compatibility with diverse functional groups makes it ideal for constructing complex heterocyclic scaffolds and API 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 : H302
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: