(R)-N-((S)-1-(2-((tert-Butyldiphenylsilyl)oxy)phenyl)-2-(diphenylphosphino)ethyl)-2-methylpropane-2-sulfinamide

95%

Reagent Code: #53881
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CAS Number 1803239-59-9

science Other reagents with same CAS 1803239-59-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 663.9200 g/mol
Formula C₄₀H₄₆NO₂PSSi
badge Registry Numbers
MDL Number MFCD32697178
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, enabling the formation of enantiomerically pure products in organic reactions. Its unique structure, featuring both sulfinamide and phosphine groups, makes it particularly effective in transition metal-catalyzed processes, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions. The tert-butyldiphenylsilyl group provides steric protection, enhancing selectivity during catalysis. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates in drug development, ensuring high enantioselectivity and yield. Additionally, its application extends to the preparation of complex natural products and fine chemicals, where precise stereocontrol is critical.

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inventory 50mg
10-20 days ฿6,300.00

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(R)-N-((S)-1-(2-((tert-Butyldiphenylsilyl)oxy)phenyl)-2-(diphenylphosphino)ethyl)-2-methylpropane-2-sulfinamide
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This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, enabling the formation of enantiomerically pure products in organic reactions. Its unique structure, featuring both sulfinamide and phosphine groups, makes it particularly effective in transition metal-catalyzed processes, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions. The tert-butyldiphenylsilyl group provides steric protection, enhancing selectivity during catalysis. It is often employed
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, enabling the formation of enantiomerically pure products in organic reactions. Its unique structure, featuring both sulfinamide and phosphine groups, makes it particularly effective in transition metal-catalyzed processes, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions. The tert-butyldiphenylsilyl group provides steric protection, enhancing selectivity during catalysis. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates in drug development, ensuring high enantioselectivity and yield. Additionally, its application extends to the preparation of complex natural products and fine chemicals, where precise stereocontrol is critical.
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