[S(R)]-N-[(S)-[2-(Dicyclohexylphosphino)phenyl]-1-naphthalenylmethyl]-2-methyl-2-propanesulfinamide

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Reagent Code: #68852
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CAS Number 2241598-30-9

science Other reagents with same CAS 2241598-30-9

blur_circular Chemical Specifications

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Weight 533.8 g/mol
Formula C₃₃H₄₄NOPS
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description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is prominent in pharmaceutical research and development, where it aids in the production of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in organic synthesis for constructing complex molecular architectures with precise stereochemical control, making it valuable in the synthesis of natural products and fine chemicals.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿1,665.00
inventory 100mg
10-20 days ฿20,691.00
inventory 500mg
10-20 days ฿102,537.00
inventory 25mg
10-20 days ฿7,191.00

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[S(R)]-N-[(S)-[2-(Dicyclohexylphosphino)phenyl]-1-naphthalenylmethyl]-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 significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is prominent in pharmaceutical research and development, where it aids in the production of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in organic synthesis for constructin

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its application is prominent in pharmaceutical research and development, where it aids in the production of chiral intermediates or active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is employed in organic synthesis for constructing complex molecular architectures with precise stereochemical control, making it valuable in the synthesis of natural products and fine chemicals.

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