(S)-1-(S)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]phosphino]-ferrocenylethyldi(3,5-xylyl)phosphine

98%

Reagent Code: #37966
fingerprint
CAS Number 1272317-38-0

science Other reagents with same CAS 1272317-38-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 910.5300 g/mol
Formula C₄₄H₃₆F₁₂FeP₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its robust structure and steric properties enhance the selectivity and efficiency of these processes, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, its ferrocene backbone contributes to stability and tunability, allowing for precise control over reaction outcomes in complex organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,052.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-1-(S)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]phosphino]-ferrocenylethyldi(3,5-xylyl)phosphine
No image available

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its robust structure and steric properties enhance the selectivity and efficiency of these processes, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, its ferrocene backbone contributes t

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its robust structure and steric properties enhance the selectivity and efficiency of these processes, making it valuable in the synthesis of pharmaceuticals and fine chemicals. Additionally, its ferrocene backbone contributes to stability and tunability, allowing for precise control over reaction outcomes in complex organic syntheses.

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...