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Structure of 419572-18-2
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exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol delivers a rigid, stereochemically defined scaffold for medicinal chemistry applications. The Boc-protected amine and pendant methanol group enable direct functionalization or derivatization under standard conditions. This bench-stable, moisture-tolerant building block integrates readily into complex molecular architectures.
exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol serves as a conformationally constrained, stereochemically defined building block for medicinal chemistry and synthetic organic applications. The Boc-protected amine enables facile deprotection under mild acidic conditions, while the terminal hydroxyl group supports orthogonal functionalization via esterification or ether formation. Its rigid bicyclic scaffold provides predictable spatial orientation, enhancing selectivity in target-directed synthesis. The compound exhibits excellent bench stability and compatibility with standard coupling and reduction protocols.
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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: