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Structure of 291775-59-2
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(1R,3S,4S)-N-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid serves as a conformationally constrained bicyclic building block for medicinal chemistry and catalytic synthesis. The Boc group provides excellent stability and ease of deprotection under mild acidic conditions. The carboxylic acid functionality enables direct coupling to amines or further derivatization, while the rigid 2-azabicyclo[2.2.1]heptane scaffold imparts defined stereochemistry and spatial orientation—ideal for probing structure-activity relationships in drug discovery and enabling efficient heterocycle formation.
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GHS Pictogram :
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GHS No : GHS07,GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H315-H319-H335-H360-H400
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Precautionary Statements : P201-P202-P260-P264-P271-P273-P280-P302+P352-P304+P340-P305+P351+P338-P308+P313-P312-P332+P313-P337+P313-P362+P364-P391-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: