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Structure of 62774-90-7
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2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid features a sterically hindered pyridine core with electron-withdrawing chlorine substituents and a methyl group at the 4-position, enhancing its utility in synthesizing bioactive heterocycles. The carboxylic acid moiety enables direct coupling reactions under standard conditions. This compound serves as a key intermediate in medicinal chemistry applications requiring halogenated, electron-deficient pyridine scaffolds.
2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyridine-based pharmaceutical intermediates. Its electron-deficient pyridine core facilitates nucleophilic substitution reactions, while the carboxylic acid and methyl groups provide orthogonal functionalization sites. The compound exhibits good bench stability and is compatible with standard coupling protocols, making it well-suited for modular scaffold construction 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: