[S(R)]-N-[(R)-[2-(Diphenylphosphino)phenyl](4-methoxyphenyl)methyl]-2-methyl-2-propanesulfinamide

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Reagent Code: #68826
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CAS Number 1595319-96-2

science Other reagents with same CAS 1595319-96-2

blur_circular Chemical Specifications

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Weight 501.6 g/mol
Formula C₃₀H₃₂NO₂PS
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description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a critical role in enantioselective transformations, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is significant in the pharmaceutical industry for the synthesis of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in academic research for developing new methodologies in organic chemistry, enabling the creation of complex molecular structures with precise stereocontrol. Its unique steric and electronic properties make it suitable for challenging asymmetric reactions, enhancing both yield and selectivity.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿36,000.00
inventory 25mg
10-20 days ฿5,886.00
inventory 100mg
10-20 days ฿9,000.00

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[S(R)]-N-[(R)-[2-(Diphenylphosphino)phenyl](4-methoxyphenyl)methyl]-2-methyl-2-propanesulfinamide
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This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a critical role in enantioselective transformations, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is significant in the pharmaceutical industry for the synthesis of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in academic research for developing new methodologies in organic chemis

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a critical role in enantioselective transformations, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is significant in the pharmaceutical industry for the synthesis of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in academic research for developing new methodologies in organic chemistry, enabling the creation of complex molecular structures with precise stereocontrol. Its unique steric and electronic properties make it suitable for challenging asymmetric reactions, enhancing both yield and selectivity.

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