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Structure of 1253924-71-8
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This spirocyclic ketone features a trifluoromethoxy-substituted phenyl ring integrated into a rigid 1,3,8-triazaspiro[4.5]dec-1-en-4-one framework, delivering enhanced metabolic stability and targeted electronic properties for use in medicinal chemistry lead optimization.
2-(4-(Trifluoromethoxy)phenyl)-1,3,8-triazaspiro[4.5]dec-1-en-4-one serves as a versatile spirocyclic building block in medicinal chemistry, enabling efficient access to complex heterocyclic scaffolds. Its conjugated enone system facilitates Michael additions and nucleophilic transformations, while the trifluoromethoxy group enhances metabolic stability and modulates lipophilicity. The triazaspiro framework provides structural rigidity and three-dimensional character, advantageous for target engagement in CNS and oncology drug discovery. Bench-stable and compatible with standard purification methods, it functions effectively 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-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: