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Structure of 230615-69-7
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This trifluoromethyl ketone derivative integrates a fused tetrahydrobenzazepine core with diamino functionality, enabling direct incorporation into bioconjugation workflows. The electron-deficient carbonyl group facilitates nucleophilic addition under mild conditions, while the trifluoromethyl moiety enhances metabolic stability and lipophilicity for targeted probe development.
1-(7,8-Diamino-1,2,4,5-tetrahydro-1,5-methano-3H-3-benzazepin-3-yl)-2,2,2-trifluoroethanone serves as a versatile building block for the synthesis of complex heterocyclic scaffolds and bioactive molecules. Its trifluoromethyl ketone functionality enables efficient imine formation and subsequent cyclization reactions, facilitating access to fused polycyclic systems. The molecule exhibits good bench stability and compatibility with common functional groups, supporting straightforward purification and integration into 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-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: