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

95%

Reagent Code: #68844
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CAS Number 2565792-78-9

science Other reagents with same CAS 2565792-78-9

blur_circular Chemical Specifications

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Weight 515.6 g/mol
Formula C₃₁H₃₄NO₂PS
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description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its application is significant in the synthesis of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. The compound's unique structure, featuring a sulfinamide group and phosphine moiety, enhances its ability to induce chirality in reaction products, making it a valuable tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,239.00
inventory 25mg
10-20 days ฿7,875.00
inventory 5mg
10-20 days ฿1,755.00

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[S(R)]-N-[(S)-[2-(Diphenylphosphino)phenyl](4-methoxyphenyl)methyl]-N,2-dimethyl-2-propanesulfinamide
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its application is significant in the synthesis of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. The compound's unique structure, featuring a sulfinamide group and phosphine moiety,

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its application is significant in the synthesis of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. The compound's unique structure, featuring a sulfinamide group and phosphine moiety, enhances its ability to induce chirality in reaction products, making it a valuable tool in organic synthesis.

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