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Structure of 35592-95-1
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2,4,6-Trichloropyridine-3,5-dicarboxylic acid features a rigid pyridine core bearing three chlorine substituents and two carboxylic acid groups at the 3 and 5 positions. This electron-deficient heterocycle serves as a robust scaffold for conjugate addition reactions and metal coordination, enabling efficient integration into functionalized materials and bioactive molecule frameworks under standard conditions.
2,4,6-Trichloropyridine-3,5-dicarboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the 3- and 5-positions via nucleophilic substitution. Its three chlorine atoms exhibit high reactivity under mild conditions, facilitating efficient coupling with amines, alcohols, and thiols to construct substituted pyridine scaffolds. The molecule’s bench-stable crystalline form and orthogonal functional group tolerance simplify purification and integration into multi-step syntheses, making it particularly valuable for medicinal chemistry and agrochemical research.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: