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Structure of 1404456-63-8
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This thiophene-based scaffold integrates a 5-chloro-2-methylpyridin-3-yl amino methyl moiety, delivering enhanced solubility and stability under standard conditions. The electron-deficient pyridine ring facilitates directed metalation, while the carboxylic acid group enables straightforward coupling reactions. Designed for modular synthesis in medicinal chemistry applications.
5-(((5-Chloro-2-methylpyridin-3-yl)amino)methyl)thiophene-2-carboxylic acid serves as a versatile building block for constructing bioactive heterocycles, enabling efficient coupling reactions via its carboxylic acid and amino functionalities. The molecule exhibits bench stability, tolerates diverse reaction conditions, and facilitates the synthesis of pharmaceutical intermediates through standard amide and Suzuki-type transformations.
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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: