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Structure of 565456-77-1
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This chiral bicyclic ester features a rigid 3-azabicyclo[3.1.0]hexane core with defined stereochemistry at the 1R,2S,5S positions, delivering predictable reactivity in asymmetric synthesis. The methyl ester group enables direct derivatization, while the hydrochloride salt enhances solubility and handling stability under standard bench conditions.
This chiral bicyclic ester serves as a versatile building block for medicinal chemistry, enabling efficient access to constrained piperidine and azabicyclic scaffolds. Its stable configuration and orthogonal functional groups facilitate downstream derivatization, including reductive amination and cross-coupling reactions. The hydrochloride salt enhances solubility and handling, supporting reliable performance in multi-step synthesis 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: