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Structure of 6729-50-6
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This tetrahydrobenzazepinone scaffold features a fused seven-membered ring with a ketone functionality, offering a rigid, electron-deficient platform for medicinal chemistry. Its bench-stable structure integrates readily into bioactive molecule design, enabling efficient access to diverse heterocyclic architectures through functionalization at the carbonyl and aromatic positions.
2,3,4,5-Tetrahydro-1H-benzo[c]azepin-1-one serves as a valuable heterocyclic building block in medicinal chemistry, offering a rigid, partially saturated scaffold with defined stereochemistry. Its ketone functionality enables direct derivatization via nucleophilic addition or reductive amination, while the fused ring system provides enhanced metabolic stability and favorable pharmacokinetic properties. The compound exhibits excellent bench stability and compatibility with standard synthetic transformations, facilitating efficient access to diverse analogs for target-directed drug discovery programs.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: