(2R,2'R,3R,3'R)-3,3'-di-tert-butyl-4,4'-diphenyl-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole

97%

Reagent Code: #36470
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CAS Number 2301856-53-9

science Other reagents with same CAS 2301856-53-9

blur_circular Chemical Specifications

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Weight 538.5960 g/mol
Formula C₃₄H₃₆O₂P₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a bibenzooxaphosphole core, makes it highly effective in inducing enantioselectivity in various organic transformations, such as hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions. The steric and electronic properties of the ligand enhance the performance of metal catalysts, enabling the synthesis of chiral molecules with high optical purity. This is particularly valuable in the pharmaceutical industry, where enantiopure compounds are often required for drug development. Additionally, its stability under reaction conditions and ease of modification make it a versatile tool in synthetic organic chemistry.

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inventory 50mg
10-20 days ฿13,257.00

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(2R,2'R,3R,3'R)-3,3'-di-tert-butyl-4,4'-diphenyl-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a bibenzooxaphosphole core, makes it highly effective in inducing enantioselectivity in various organic transformations, such as hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions. The steric and electronic properties of the ligand enhance the performance of metal catalysts, enabling the synthesis of chiral molecules w

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a bibenzooxaphosphole core, makes it highly effective in inducing enantioselectivity in various organic transformations, such as hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions. The steric and electronic properties of the ligand enhance the performance of metal catalysts, enabling the synthesis of chiral molecules with high optical purity. This is particularly valuable in the pharmaceutical industry, where enantiopure compounds are often required for drug development. Additionally, its stability under reaction conditions and ease of modification make it a versatile tool in synthetic organic chemistry.

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