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Structure of 215453-53-5
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7-Bromoisoquinolin-1-amine delivers a brominated isoquinoline scaffold with a primary amine at the 1-position, enabling direct functionalization in cross-coupling and medicinal chemistry applications. The electron-deficient ring system enhances reactivity in palladium-catalyzed transformations, while the pendant amine offers versatility for derivatization. This bench-stable, moisture-tolerant heterocycle serves as a key building block for kinase inhibitors and bioactive alkaloid analogs.
7-Bromoisoquinolin-1-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C7 position via palladium-catalyzed cross-coupling reactions. The amine group facilitates conjugation and derivatization, while the bromide offers orthogonal reactivity for late-stage modifications. Its stability under standard synthetic conditions and compatibility with diverse transformations make it ideal for constructing complex heterocyclic scaffolds in API development.
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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: