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Structure of 1086382-78-6
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2-Bromo-5-cyclopropylpyrazine features a cyclopropyl group that enhances lipophilicity and metabolic stability, while the bromine substituent enables facile cross-coupling reactions. This scaffold integrates readily into diverse heterocyclic architectures under standard conditions, offering a robust platform for medicinal chemistry and materials synthesis.
2-Bromo-5-cyclopropylpyrazine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to construct biaryl and heteroaryl scaffolds. The bromine atom facilitates efficient functionalization under standard Suzuki, Stille, or Negishi conditions, while the cyclopropyl group enhances metabolic stability and modulates lipophilicity. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for iterative synthesis of complex heterocyclic systems.
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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: