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Structure of 150969-56-5
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5-Trifluoromethyl-1-indanone features a sterically constrained indanone core bearing a strongly electron-withdrawing trifluoromethyl group at the 5-position, enhancing electrophilicity at the carbonyl center. This configuration supports efficient Michael additions and conjugate functionalizations under mild conditions, making it valuable for constructing complex heterocycles and bioactive scaffolds in medicinal chemistry and materials synthesis.
5-Trifluoromethyl-1-indanone serves as a versatile building block in medicinal chemistry, enabling efficient construction of indanone-based scaffolds through standard carbonyl transformations. Its trifluoromethyl group enhances metabolic stability and modulates lipophilicity, while the fused bicyclic structure provides rigidity advantageous for target binding. The compound exhibits excellent bench stability and facilitates straightforward functionalization via nucleophilic addition or transition-metal-catalyzed coupling reactions.
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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: