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Structure of 1246509-66-9
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This chiral indene derivative features a stereodefined (3S) amino group and a bench-stable methyl ester, enabling direct incorporation into peptide-like scaffolds. The hydrochloride salt enhances solubility and handling in aqueous reaction media.
(3S)-3-Amino-2,3-dihydro-1H-indene-5-carboxylic acid methyl ester hydrochloride serves as a stereochemically defined building block for indoline-based pharmaceutical intermediates. The chiral center at C3 ensures enantioselective access to bioactive scaffolds, while the amino and ester functionalities enable diverse transformations including amidation, cyclization, and metal-catalyzed coupling. Bench-stable and readily purified, it functions effectively in standard peptide-like syntheses and heterocycle construction 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: