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Structure of 1197595-75-7
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This bench-stable indenamine derivative features a brominated aromatic core and a protonated amine, enabling straightforward incorporation into transition metal-catalyzed cross-coupling reactions. The hydrochloride salt enhances solubility in polar solvents, facilitating use in synthetic workflows requiring precise nitrogen delivery.
5-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to indoline scaffolds via palladium-catalyzed cross-coupling and electrophilic functionalization. The bromo group facilitates C–C and C–N bond formation under standard conditions, while the amine functionality provides a handle for derivatization and salt formation. Its bench-stable crystalline form supports straightforward handling and purification, making it well-suited for iterative synthesis workflows and API intermediate development.
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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: