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Structure of 1891002-61-1
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This chiral phosphole features a sterically shielded tert-butyl group and an anthracen-9-yl moiety, delivering enhanced stability and defined stereochemistry. The isopropyl substituent improves solubility, while the fused oxaphosphole core enables efficient coordination in asymmetric catalysis. Bench-stable under standard conditions, it integrates readily into transition-metal-mediated transformations.
(2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2-isopropyl-2,3-dihydrobenzo[d][1,3]oxaphosphole serves as a stereodefined phosphole scaffold with enhanced bench stability and functional group tolerance. Its anthracenyl moiety enables π-extended conjugation for applications in photoreactive or electron-transport materials, while the tert-butyl and isopropyl substituents provide steric shielding and facilitate purification. The molecule functions as a versatile building block in asymmetric synthesis and transition-metal catalysis, particularly in Pd-catalyzed cross-coupling processes requiring stable, chiral phosphorus ligands.
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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: