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Structure of 1632-68-4
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Bicyclo[2.2.1]heptan-2-ol offers a rigid, bridged scaffold ideal for stereocontrolled synthesis. The hydroxyl group at the bridgehead position enables direct functionalization while maintaining structural integrity. This bench-stable compound integrates readily into complex molecular architectures requiring defined three-dimensional geometry and predictable reactivity patterns.
Bicyclo[2.2.1]heptan-2-ol serves as a rigid, chiral scaffold in synthetic organic chemistry, enabling stereocontrolled transformations through its well-defined bridgehead stereocenter. Its bench-stable nature and compatibility with diverse functional groups facilitate efficient access to complex polycyclic architectures. This compound functions as a key building block in the synthesis of natural products and pharmaceutical intermediates, particularly where conformational constraint and defined spatial orientation are essential.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: