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Structure of 1696988-00-7
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5-Bromo-3-chloro-8-methoxyisoquinoline features a halogenated isoquinoline core with strategically positioned bromo, chloro, and methoxy substituents. This electron-deficient scaffold enables efficient coupling in cross-coupling reactions, particularly in Pd-catalyzed transformations. The methoxy group enhances solubility and modulates reactivity, while the ortho-halogen pattern supports sequential functionalization. Bench-stable and moisture-tolerant, it serves as a robust building block for medicinal chemistry and materials science applications.
5-Bromo-3-chloro-8-methoxyisoquinoline serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. The bromo group enables palladium-catalyzed coupling with boronic acids, stannanes, or amines, while the chloro substituent offers orthogonal reactivity for sequential functionalization. The methoxy group enhances solubility and modulates electronic properties. This compound exhibits excellent bench stability and is compatible with standard purification methods, facilitating efficient synthesis of complex isoquinoline-based scaffolds.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: