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Structure of 913836-18-7
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Methyl 2-iodonicotinate is a bench-stable, moisture-tolerant iodinated pyridine derivative featuring a strategically positioned ester group. This compound integrates readily into cross-coupling workflows, serving as a direct precursor for C–C bond formation at the pyridine 2-position. The iodine moiety enables efficient palladium-catalyzed transformations under standard conditions.
Methyl 2-iodonicotinate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable iodide functionality. Its pyridine core provides orthogonal reactivity for late-stage functionalization, while the ester group offers compatibility with standard reduction and derivatization protocols. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to substituted nicotinates and heterocyclic scaffolds relevant to medicinal chemistry and agrochemical development.
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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-P501
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Lot numbers can be found on the outside label of a product: