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Structure of 312753-53-0
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This bench-stable indenamine derivative features two ethyl substituents at the 5,6-positions, enhancing lipophilicity and metabolic stability. The protonated amine group ensures water solubility and facilitates salt formation, enabling efficient handling in synthetic workflows.
5,6-Diethyl-2,3-dihydro-1H-inden-2-amine hydrochloride serves as a stable, bench-ready building block for indoline-based scaffolds. Its amine functionality enables straightforward derivatization in amide coupling, reductive amination, and electrophilic substitution reactions. The diethyl substitution enhances lipophilicity and metabolic stability, making it suitable for medicinal chemistry campaigns targeting CNS-active compounds. The hydrochloride salt improves solubility and handling, facilitating purification and integration into standard synthetic 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-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: