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Structure of 2351219-90-2
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This chiral phosphole features a sterically shielded tert-butyl group and an electron-rich aryl moiety with dual methoxy and isopropyl substituents, enabling robust coordination in asymmetric catalysis. Its bench-stable, moisture-tolerant structure simplifies handling in air-sensitive transformations.
(R)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole serves as a sterically encumbered, bench-stable phosphole scaffold enabling efficient transition-metal-catalyzed cross-coupling reactions. Its ortho-dimethoxy substitution enhances electronic modulation and solubility, while the chiral tertiary phosphorus center provides stereochemical control in asymmetric synthesis. Functions effectively in Pd-catalyzed coupling protocols and acts as a versatile building block for bioactive heterocyclic systems.
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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: