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Structure of 1260665-75-5
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5-Chloro-3-methylpyrazine-2-carbonitrile features a pyrazine core functionalized with chlorine, methyl, and nitrile groups, enabling direct integration into heterocyclic scaffolds. The electron-deficient ring facilitates nucleophilic substitution, while the nitrile group serves as a handle for downstream derivatization. This compound demonstrates stability under standard bench conditions and is compatible with common synthetic protocols in medicinal chemistry and materials science.
5-Chloro-3-methylpyrazine-2-carbonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrazine scaffolds. Its complementary electron-withdrawing nitrile and chloro groups facilitate palladium-catalyzed cross-coupling reactions, while the methyl substituent provides a handle for further functionalization. The compound exhibits good bench stability and is compatible with standard synthetic workflows, making it a practical choice for medicinal chemistry and process development applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: