(S)-1-[(S)-tert-Butylphosphinoyl]-2-[(S)-1-(diphenylphosphino)ethyl]ferrocene

98%

Reagent Code: #68674
fingerprint
CAS Number 1221746-31-1

science Other reagents with same CAS 1221746-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 502.35 g/mol
Formula C₂₈H₃₂FeOP₂
badge Registry Numbers
MDL Number MFCD18827473
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

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 enantioselective synthesis, enabling the production of chiral compounds with high optical purity. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it is employed in the synthesis of fine chemicals and agrochemicals, where the control of stereochemistry is essential for the desired biological activity. The unique ferrocene backbone and phosphine groups in this ligand contribute to its stability and effectiveness in various catalytic processes, including hydrogenation, cross-coupling, and carbon-carbon bond formation reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,291.00
inventory 1g
10-20 days ฿38,160.00
inventory 100mg
10-20 days ฿6,336.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-1-[(S)-tert-Butylphosphinoyl]-2-[(S)-1-(diphenylphosphino)ethyl]ferrocene
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of chiral compounds with high optical purity. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it is employed in the

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of chiral compounds with high optical purity. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it is employed in the synthesis of fine chemicals and agrochemicals, where the control of stereochemistry is essential for the desired biological activity. The unique ferrocene backbone and phosphine groups in this ligand contribute to its stability and effectiveness in various catalytic processes, including hydrogenation, cross-coupling, and carbon-carbon bond formation reactions.

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...