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Structure of 298693-03-5
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This chiral bisoxazole features a rigid cyclopentylidene bridge enabling precise spatial control in asymmetric synthesis. The tert-butyl groups provide steric shielding and enhanced solubility, while the dihydrooxazole rings offer stable, electron-rich coordination sites. Ideal for constructing enantioselective ligands and catalysts in transition metal catalysis.
(4S,4'S)-2,2'-Cyclopentylidenebis[4-tert-butyl-4,5-dihydrooxazole] serves as a chiral, bench-stable auxiliary for asymmetric synthesis, enabling stereoselective C–C and C–heteroatom bond formation. Its rigid cyclopentylidene backbone imparts high diastereoselectivity in nucleophilic additions and enolate alkylations, while the 4-tert-butyl oxazole groups enhance solubility and simplify purification. Functions reliably in standard organic transformations without requiring inert conditions.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: