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*For research and further manufacturing use only, not for direct human use.
Structure of 1532-24-7
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Methyl 3,6-dichloropicolinate is a bench-stable heterocyclic ester featuring two chlorine atoms at the 3- and 6-positions of the picolinic acid core. This electron-deficient scaffold integrates readily into synthetic sequences requiring halogenated pyridine motifs. The methyl ester group enables direct functionalization or hydrolysis to the corresponding carboxylic acid under standard conditions.
Methyl 3,6-dichloropicolinate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted pyridine scaffolds via cross-coupling and functional group interconversion. Its dual chloro substituents provide orthogonal reactivity for sequential transformations, while the ester group facilitates downstream derivatization. The compound exhibits excellent bench stability and is compatible with standard reaction conditions, making it well-suited for medicinal chemistry campaigns and process-scale synthesis.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: