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Structure of 69422-72-6
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2,4,6-Trichloronicotinic acid features a highly electron-deficient pyridine ring stabilized by three chlorine substituents at the 2, 4, and 6 positions. This configuration enhances its utility as a building block in synthetic routes requiring strong inductive withdrawal or directed metalation. The compound exhibits robust bench stability and compatibility with standard organic reaction conditions.
2,4,6-Trichloronicotinic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, offering high reactivity at the carboxylic acid functional group. Its electron-deficient pyridine core facilitates nucleophilic aromatic substitution and enables efficient derivatization under mild conditions. The molecule exhibits excellent bench stability and simplifies purification due to its crystalline nature, making it well-suited for scale-up applications in API 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: