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Structure of 67120-39-2
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5-Chloro-1-indanylamine features a chlorine-substituted indane scaffold with a primary amine at the 1-position, offering enhanced electron density and steric profile for targeted functionalization. This bench-stable derivative serves as a key intermediate in pharmaceutical synthesis, particularly for CNS-active compounds and kinase inhibitors.
5-Chloro-1-indanylamine serves as a valuable building block for indoline-based scaffolds in medicinal chemistry. Its amine functionality enables straightforward derivatization via acylation, alkylation, or reductive amination, while the chloro substituent offers a handle for palladium-catalyzed cross-coupling reactions. The molecule exhibits good bench stability and is compatible with standard purification methods, facilitating integration into multi-step synthetic sequences targeting CNS-active compounds and kinase inhibitors.
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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: