(11aS)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine

98%

Reagent Code: #36155
fingerprint
CAS Number 486429-92-9

science Other reagents with same CAS 486429-92-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 566.5646 g/mol
Formula C₃₇H₂₈O₂P₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(11aS)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine is primarily used as a chiral ligand in asymmetric catalysis. It plays a significant role in facilitating enantioselective reactions, particularly in the synthesis of complex organic molecules. This compound is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantioselectivity is required. Its unique structure and chiral properties make it valuable in the pharmaceutical industry for producing enantiomerically pure drugs. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore novel synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,520.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(11aS)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine
No image available

(11aS)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine is primarily used as a chiral ligand in asymmetric catalysis. It plays a significant role in facilitating enantioselective reactions, particularly in the synthesis of complex organic molecules. This compound is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantioselectivity is required. Its unique structure and chiral properties make it valuable in the

(11aS)-1,11-Bis(diphenylphosphino)dibenzo[d,f][1,3]dioxepine is primarily used as a chiral ligand in asymmetric catalysis. It plays a significant role in facilitating enantioselective reactions, particularly in the synthesis of complex organic molecules. This compound is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantioselectivity is required. Its unique structure and chiral properties make it valuable in the pharmaceutical industry for producing enantiomerically pure drugs. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore novel synthetic pathways.

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...