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Structure of 2757082-23-6
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This indeno[1,2-d]oxazole features a trifluoromethylpyridine moiety that enhances electron deficiency and metabolic stability. The fused bicyclic scaffold provides rigidity and improved binding affinity, making it suitable for medicinal chemistry applications requiring enhanced lipophilicity and target engagement under physiological conditions.
(3aS,8aR)-2-(5-(Trifluoromethyl)pyridin-2-yl)-8,8a-dihydro-3aH-indeno[1,2-d]oxazole serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to complex fused scaffolds. Its rigid, planar architecture and electron-deficient trifluoromethylpyridine moiety enhance binding affinity in target-directed synthesis. The indeno[1,2-d]oxazole core exhibits excellent bench stability, tolerates diverse functional groups, and facilitates downstream transformations via electrophilic or transition-metal-catalyzed coupling reactions, making it well-suited for high-throughput screening and API development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: