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Structure of 1030829-21-0
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Methyl 6-chloro-3-fluoropicolinate features a strategically positioned chloro and fluoro substituent on the picolinate scaffold, enabling enhanced electrophilicity at the carbonyl carbon. This electron-deficient heterocycle integrates readily into transition-metal-catalyzed coupling reactions, offering high functional group tolerance and stability under standard conditions.
Methyl 6-chloro-3-fluoropicolinate serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its ortho-substituted pyridine core facilitates transition metal-catalyzed cross-coupling reactions, while the methyl ester group supports selective derivatization. The molecule exhibits excellent bench stability and compatibility with diverse functional groups, simplifying purification and integration into multi-step synthetic sequences.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: