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Structure of 2097145-90-7
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This bicyclic oxazole scaffold features a rigid, sterically defined core with dual indeno-oxazole units linked by a cyclobutylidene bridge. The configuration at the chiral centers imparts high structural integrity and predictable stereochemical behavior. Designed for use in asymmetric synthesis and molecular recognition applications, it offers enhanced stability under standard bench conditions and facilitates precise spatial control in catalytic or ligand systems.
(3aR,3'aR,8aS,8'aS)-2,2'-Cyclobutylidenebis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole] serves as a rigid, chiral bis-heterocyclic scaffold enabling precise spatial control in asymmetric synthesis. Its fused indeno-oxazole framework exhibits excellent bench stability and functional group tolerance, facilitating use in transition-metal-catalyzed coupling reactions and as a building block for complex polycyclic systems. The molecule functions effectively as a ligand precursor or auxiliary in stereoselective transformations.
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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: