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Structure of 188780-32-7
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This chiral bis-oxazole features a rigid, fused indenyl bridge enabling precise spatial control in asymmetric synthesis. The 4,5-dihydrooxazole rings offer enhanced stability and solubility, while the phenyl substituents provide π-conjugation and steric modulation. Ideal for ligand design and catalytic applications requiring defined stereochemistry and robust handling under standard conditions.
(4S,4'S)-2,2'-(1,3-Dihydro-2H-inden-2-ylidene)bis[4,5-dihydro-4-phenyloxazole] serves as a chiral bis-oxazole scaffold with defined stereochemistry at the indenyl bridge, enabling controlled spatial orientation in asymmetric synthesis. Its rigid, planar architecture facilitates π–π stacking interactions and provides orthogonal functional handles for downstream derivatization. The molecule exhibits excellent bench stability, clean purification profiles, and compatibility with standard coupling and reduction protocols, making it a robust building block for complex heterocyclic systems and molecular scaffolds in medicinal chemistry applications.
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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: