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Structure of 630421-73-7
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1,6-Dichloro-isoquinoline features two chlorine atoms positioned at the 1- and 6-locations of the isoquinoline core, conferring enhanced electrophilicity and stability. This electron-deficient scaffold integrates readily into cross-coupling reactions, enabling efficient construction of complex heterocyclic architectures in medicinal chemistry and materials science applications.
1,6-Dichloro-isoquinoline serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions at both chlorine sites. Its stability under standard reaction conditions and orthogonal reactivity facilitate sequential functionalization for the construction of complex isoquinoline-based scaffolds. The molecule functions effectively in late-stage diversification efforts within medicinal chemistry and materials science 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-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: