[S(R)]-N-[(1R)-1-[2-((tert-Butyldiphenylsilyl)oxy)phenyl)]-2-yl-2-(diphenylphosphino)ethyl]-2-methyl-2-propanesulfinamide

≥95%

Reagent Code: #65014
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CAS Number 1803239-58-8

science Other reagents with same CAS 1803239-58-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 663.9299999999999 g/mol
Formula C₄₀H₄₆NO₂PSSi
badge Registry Numbers
MDL Number MFCD32697179
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This chemical is primarily used in asymmetric synthesis, particularly in the formation of chiral compounds. It serves as a chiral ligand or catalyst in various organic reactions, including enantioselective hydrogenation and carbon-carbon bond formation. Its structure, featuring a diphenylphosphino group and a sulfinamide moiety, makes it effective in controlling stereochemistry, enabling the production of optically active molecules. This is especially valuable in pharmaceutical synthesis, where the chirality of a drug can significantly impact its efficacy and safety. Additionally, it is utilized in research and development for creating complex molecular architectures with high precision.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿2,241.00
inventory 25mg
10-20 days ฿8,631.00

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[S(R)]-N-[(1R)-1-[2-((tert-Butyldiphenylsilyl)oxy)phenyl)]-2-yl-2-(diphenylphosphino)ethyl]-2-methyl-2-propanesulfinamide
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This chemical is primarily used in asymmetric synthesis, particularly in the formation of chiral compounds. It serves as a chiral ligand or catalyst in various organic reactions, including enantioselective hydrogenation and carbon-carbon bond formation. Its structure, featuring a diphenylphosphino group and a sulfinamide moiety, makes it effective in controlling stereochemistry, enabling the production of optically active molecules. This is especially valuable in pharmaceutical synthesis, where the chira

This chemical is primarily used in asymmetric synthesis, particularly in the formation of chiral compounds. It serves as a chiral ligand or catalyst in various organic reactions, including enantioselective hydrogenation and carbon-carbon bond formation. Its structure, featuring a diphenylphosphino group and a sulfinamide moiety, makes it effective in controlling stereochemistry, enabling the production of optically active molecules. This is especially valuable in pharmaceutical synthesis, where the chirality of a drug can significantly impact its efficacy and safety. Additionally, it is utilized in research and development for creating complex molecular architectures with high precision.

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