(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-4,4'-bis(2,6-dimethoxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole

97%,≥99% ee

Reagent Code: #96546
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CAS Number 1435940-21-8

science Other reagents with same CAS 1435940-21-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 658.7 g/mol
Formula C₃₈H₄₄O₆P₂
badge Registry Numbers
MDL Number MFCD31707598
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry make it highly effective in inducing enantioselectivity, which is crucial for producing chiral compounds in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other enantioselective transformations, enabling the synthesis of complex molecules with high optical purity. Additionally, its stability and efficiency under various reaction conditions make it a valuable tool in organic synthesis and industrial applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,291.00
inventory 500mg
10-20 days ฿71,991.00
inventory 100mg
10-20 days ฿15,480.00

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(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-4,4'-bis(2,6-dimethoxyphenyl)-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 and stereochemistry make it highly effective in inducing enantioselectivity, which is crucial for producing chiral compounds in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other enantioselective transformations, enabling the synthesis of complex molecules with high optical puri

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry make it highly effective in inducing enantioselectivity, which is crucial for producing chiral compounds in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other enantioselective transformations, enabling the synthesis of complex molecules with high optical purity. Additionally, its stability and efficiency under various reaction conditions make it a valuable tool in organic synthesis and industrial applications.

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