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Structure of 1309359-79-2
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tert-Butyl 5-oxoazocane-1-carboxylate features a stable, bench-stable cyclic ketone embedded within a nine-membered ring framework. This compound integrates a protected carboxylic acid group that enables selective transformations in complex molecular architectures. The sterically shielded tert-butyl ester facilitates clean deprotection under mild conditions, while the oxo function serves as a pivotal handle for reductive functionalization or nucleophilic addition.
tert-Butyl 5-oxoazocane-1-carboxylate serves as a versatile scaffold for the synthesis of nitrogen-containing heterocycles and bioactive molecules. Its ketone functionality enables efficient enolate formation and subsequent C–C bond construction, while the tert-butyl ester group offers robust protection with facile removal under mild acidic conditions. The molecule exhibits excellent bench stability and compatibility with diverse functional groups, facilitating its use in multi-step synthetic sequences.
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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
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Precautionary Statements : P264-P270-P280-P301+P310-P302+P352-P305+P351+P338-P330-P332+P313-P337+P313-P362+P364-P501
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Lot numbers can be found on the outside label of a product: