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Structure of 2435-46-3
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3,6-Dimethylpyrazine-2-carboxylic acid features a rigid pyrazine core functionalized with methyl and carboxylic acid groups at strategic positions, enabling direct integration into bioactive scaffolds. The electron-deficient ring system enhances reactivity in coupling reactions, while the carboxylic acid moiety facilitates derivatization under standard conditions. This structure supports applications in medicinal chemistry and materials science, where controlled polarity and stability are essential.
3,6-Dimethylpyrazine-2-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its pyrazine core provides robust stability and orthogonal reactivity, enabling direct functionalization at the carboxylic acid and methyl groups. The compound facilitates coupling reactions, derivatization, and incorporation into bioactive scaffolds with predictable stereochemical outcomes. Bench-stable and readily purified by recrystallization, it functions reliably in standard synthetic workflows.
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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: