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Structure of 1884594-03-9
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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 ethyl substituent at the 2-position improves solubility and facilitates handling under standard conditions. Designed for asymmetric synthesis, this bench-stable oxaphosphole integrates readily into catalytic systems requiring precise spatial control.
(2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2-ethyl-2,3-dihydrobenzo[d][1,3]oxaphosphole serves as a chiral, sterically encumbered phosphole ligand that facilitates asymmetric transition-metal-catalyzed transformations. Its rigid fused oxaphosphole core and bulky tert-butyl group enhance stereocontrol in palladium- and nickel-catalyzed cross-couplings. The anthracenyl moiety contributes π-conjugation and electronic modulation, while the ethyl substituent improves solubility and handling. This ligand demonstrates robust performance in standard Buchwald–Hartwig amination protocols and exhibits high bench stability under ambient 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: