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Structure of 1638771-06-8
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tert-Butyl N-{3-formylbicyclo[1.1.1]pentan-1-yl}carbamate features a rigid, electron-deficient bicyclic core paired with a formyl group at the 3-position, enabling direct functionalization in complex molecular architectures. The tert-butyl carbamate moiety provides stability and convenient deprotection under mild acidic conditions. This combination supports rapid access to constrained scaffolds in medicinal chemistry and fragment-based drug discovery.
tert-Butyl N-{3-formylbicyclo[1.1.1]pentan-1-yl}carbamate serves as a versatile building block in synthetic organic chemistry, leveraging the rigid bicyclo[1.1.1]pentane scaffold for three-dimensional molecular design. The formyl group enables direct functionalization via reductive amination, oxime formation, or nucleophilic addition, while the tert-butyl carbamate provides a stable, easily removable protecting group. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient incorporation into complex architectures, including medicinal chemistry lead optimization and macrocyclic scaffold construction.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: