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

95%

Reagent Code: #68849
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CAS Number 2249950-31-8

science Other reagents with same CAS 2249950-31-8

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Weight 637.9 g/mol
Formula C₄₁H₅₂NOPS
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description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a crucial role in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals where high enantiomeric purity is essential. Its unique structure, combining diadamantanphosphino and sulfinamide groups, enhances its ability to induce chirality in various organic transformations, such as hydrogenation, cross-coupling, and addition reactions. This makes it valuable in the development of drugs, agrochemicals, and other biologically active molecules with specific stereochemical requirements.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿71,901.00
inventory 100mg
10-20 days ฿20,160.00

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[S(R)]-N-[(R)-[2-(Diadamantanphosphino)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 crucial role in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals where high enantiomeric purity is essential. Its unique structure, combining diadamantanphosphino and sulfinamide groups, enhances its ability to induce chirality in various organic transformations, such as hydrogenation, cross-coupling, and addition reactions. This makes it valu

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a crucial role in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals where high enantiomeric purity is essential. Its unique structure, combining diadamantanphosphino and sulfinamide groups, enhances its ability to induce chirality in various organic transformations, such as hydrogenation, cross-coupling, and addition reactions. This makes it valuable in the development of drugs, agrochemicals, and other biologically active molecules with specific stereochemical requirements.

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