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Structure of 229184-97-8
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This chiral oxazole dimer features a rigid cyclopropylidene bridge that enforces a defined spatial arrangement, enabling precise stereocontrol in asymmetric synthesis. The diphenyl-substituted oxazole rings provide enhanced stability and solubility in organic media, facilitating use in catalytic applications.
(4S,4'S,5R,5'R)-2,2'-Cyclopropylidenebis[4,5-dihydro-4,5-diphenyloxazole] serves as a chiral, rigid bis-oxazole scaffold enabling asymmetric synthesis of complex heterocyclic systems. Its defined stereochemistry and stability under standard reaction conditions facilitate predictable coupling reactions, while the diphenyl-substituted oxazole rings offer enhanced functional group tolerance and ease of purification. This compound functions effectively in transition metal-catalyzed transformations and acts as a valuable building block for medicinal chemistry campaigns requiring conformationally constrained architectures.
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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: