Bis(3,5-bis(trifluoromethyl)phenyl)(2',6'-bis(dimethylamino)-3,6-dimethoxybiphenyl-2-yl)phosphine

≥95%

Reagent Code: #68742
fingerprint
CAS Number 1810068-30-4

science Other reagents with same CAS 1810068-30-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 756.5599999999999 g/mol
Formula C₃₄H₂₉F₁₂N₂O₂P
thermostat Physical Properties
Melting Point 160.3°C
Boiling Point 611.2±55.0℃(Predicted)
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its electron-rich and sterically hindered structure enhances the stability and reactivity of the metal complexes, enabling efficient catalytic cycles. It is especially valuable in synthesizing complex organic molecules, including pharmaceuticals and fine chemicals, where high selectivity and yield are critical. The trifluoromethyl groups contribute to the ligand's solubility in organic solvents, facilitating its use in homogeneous catalysis. Additionally, its unique steric and electronic properties make it suitable for challenging transformations that require precise control over reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿83,286.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Bis(3,5-bis(trifluoromethyl)phenyl)(2',6'-bis(dimethylamino)-3,6-dimethoxybiphenyl-2-yl)phosphine
No image available

This chemical is primarily utilized as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its electron-rich and sterically hindered structure enhances the stability and reactivity of the metal complexes, enabling efficient catalytic cycles. It is especially valuable in synthesizing complex organic molecules, including pharmaceuticals and fine chemicals, where high selectivity and yield are critical. The trifluo

This chemical is primarily utilized as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its electron-rich and sterically hindered structure enhances the stability and reactivity of the metal complexes, enabling efficient catalytic cycles. It is especially valuable in synthesizing complex organic molecules, including pharmaceuticals and fine chemicals, where high selectivity and yield are critical. The trifluoromethyl groups contribute to the ligand's solubility in organic solvents, facilitating its use in homogeneous catalysis. Additionally, its unique steric and electronic properties make it suitable for challenging transformations that require precise control over reaction conditions.

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...