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Structure of 1246509-67-0
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This chiral indene derivative features a bench-stable, moisture-tolerant methyl ester group and a protonated amine, enabling straightforward coupling and derivatization. The (3R) configuration ensures high stereochemical fidelity in asymmetric synthesis, while the para-carboxylate functionality facilitates conjugation and solubility optimization in biopharmaceutical workflows.
(3R)-3-Amino-2,3-dihydro-1H-indene-5-carboxylic acid methyl ester hydrochloride serves as a stereochemically defined building block for indoline-based scaffolds. The chiral center at C3 ensures high enantioselectivity in downstream transformations, while the amino and ester functionalities enable sequential derivatization—facilitating amide coupling, reductive amination, or cyclization reactions. Bench-stable and readily purified by standard techniques, it functions effectively in medicinal chemistry campaigns 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: