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Structure of 731859-02-2
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(1R)-6-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride offers a chiral, electron-deficient indenyl scaffold ideal for asymmetric synthesis. This bench-stable salt features a rigid, fused bicyclic core with a fluorine substituent at the 6-position, enhancing metabolic stability and modulating electronic properties. The primary amine functionality enables straightforward derivatization, facilitating incorporation into bioactive scaffolds and catalyst systems.
(1R)-6-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride serves as a chiral building block for the synthesis of bioactive indoline derivatives. Its fluorinated aromatic core provides enhanced metabolic stability and modulated electronic properties, while the secondary amine functionality enables straightforward derivatization via reductive amination, acylation, or coupling reactions. The hydrochloride salt enhances solubility and handling stability, facilitating use in standard medicinal chemistry workflows.
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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-H319
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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: