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Structure of 313340-08-8
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3,5-Dichloro-6-ethylpyrazine-2-carboxamide features a pyrazine core functionalized with chlorine substituents at positions 3 and 5, an ethyl group at 6, and a carboxamide at 2. This electron-deficient heterocycle integrates readily into medicinal chemistry scaffolds, offering enhanced metabolic stability and favorable binding interactions in target-directed synthesis.
3,5-Dichloro-6-ethylpyrazine-2-carboxamide serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of pyrazine-based scaffolds through standard amide coupling and electrophilic substitution reactions. Its dichloro substituents provide orthogonal reactivity for late-stage functionalization, while the ethyl and carboxamide groups offer favorable solubility and stability under routine synthetic conditions. This compound facilitates the synthesis of bioactive molecules with enhanced metabolic profile and is well-suited for parallel library generation in drug discovery 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: