[S(R)]-N-[(1R)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methyl-2-propanesulfinamide

95%

Reagent Code: #68831
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CAS Number 1595319-89-3

science Other reagents with same CAS 1595319-89-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.5 g/mol
Formula C₂₄H₂₈NOPS
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description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic asymmetric hydrogenation reactions. It plays a crucial role in the production of enantiomerically pure compounds, which are essential in the pharmaceutical industry for the development of drugs with specific stereochemical requirements. Its application extends to the synthesis of complex organic molecules, where it helps in achieving high enantioselectivity and yield. Additionally, it is employed in the preparation of chiral catalysts for various organic transformations, contributing to advancements in medicinal chemistry and fine chemical manufacturing.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿7,407.00
100mg
10-20 days ฿21,312.00
500mg
10-20 days ฿54,000.00
[S(R)]-N-[(1R)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methyl-2-propanesulfinamide
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This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic asymmetric hydrogenation reactions. It plays a crucial role in the production of enantiomerically pure compounds, which are essential in the pharmaceutical industry for the development of drugs with specific stereochemical requirements. Its application extends to the synthesis of complex organic molecules, where it helps in achieving high enantioselectivity and yield. Additionally, it is employed in the
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic asymmetric hydrogenation reactions. It plays a crucial role in the production of enantiomerically pure compounds, which are essential in the pharmaceutical industry for the development of drugs with specific stereochemical requirements. Its application extends to the synthesis of complex organic molecules, where it helps in achieving high enantioselectivity and yield. Additionally, it is employed in the preparation of chiral catalysts for various organic transformations, contributing to advancements in medicinal chemistry and fine chemical manufacturing.
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