[S(R)]-N-[(S)-[3,5-Bis(1,1-dimethylethyl)-4-methoxyphenyl][2-(diphenylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide

95%

Reagent Code: #68853
fingerprint
CAS Number 1616688-63-1

science Other reagents with same CAS 1616688-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 613.8 g/mol
Formula C₃₈H₄₈NO₂PS
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure drugs, where the specific spatial arrangement of atoms can significantly influence the drug's efficacy and safety. Additionally, it finds application in the synthesis of complex organic molecules, enabling the creation of compounds with precise stereochemistry for use in advanced materials and fine chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿43,200.00
inventory 25mg
10-20 days ฿7,875.00
inventory 100mg
10-20 days ฿10,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
[S(R)]-N-[(S)-[3,5-Bis(1,1-dimethylethyl)-4-methoxyphenyl][2-(diphenylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide
No image available

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure drugs, where the specific spatial arrangement of atoms can significantly influence the drug's efficac

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure drugs, where the specific spatial arrangement of atoms can significantly influence the drug's efficacy and safety. Additionally, it finds application in the synthesis of complex organic molecules, enabling the creation of compounds with precise stereochemistry for use in advanced materials and fine chemicals.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...