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Structure of 1358991-52-2
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This isoindoline scaffold features two chiral oxazoline moieties positioned at the 1,3-positions, creating a rigid, electron-deficient framework ideal for asymmetric catalysis. The (1Z,3Z) configuration ensures optimal spatial orientation for transition-metal coordination and substrate recognition in enantioselective transformations.
(1Z,3Z)-1,3-Bis(((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methylene)isoindoline serves as a versatile chiral bis-oxazoline scaffold, enabling selective coordination in asymmetric catalysis. Its rigid, planar architecture supports efficient metal binding and stereocontrol in transition-metal-catalyzed transformations. The molecule exhibits bench stability, tolerates diverse functional groups, and facilitates purification via standard chromatographic methods—making it well-suited for iterative synthesis of complex heterocyclic systems and catalyst development in industrial R&D settings.
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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: