1,1'-[(1R)-6,6'-Dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis[1,1-bis(4-chlorophenyl)phosphine]

98%

Reagent Code: #65720
fingerprint
CAS Number 1310054-04-6

science Other reagents with same CAS 1310054-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 720.4 g/mol
Formula C₃₈H₂₈Cl₄O₂P₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a chiral ligand in transition metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Its unique structure, featuring biphenyl and bis(4-chlorophenyl)phosphine groups, allows it to effectively coordinate with metals like rhodium or iridium, enhancing the efficiency and selectivity of the catalytic system. Applications include the production of chiral pharmaceuticals, fine chemicals, and agrochemicals, where precise stereocontrol is critical. Its stability and ability to induce high enantiomeric excess make it a valuable tool in advanced organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿18,756.00
inventory 10mg
10-20 days ฿4,698.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,1'-[(1R)-6,6'-Dimethoxy[1,1'-biphenyl]-2,2'-diyl]bis[1,1-bis(4-chlorophenyl)phosphine]
No image available
This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a chiral ligand in transition metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Its unique structure, featuring biphenyl and bis(4-chlorophenyl)phosphine groups, allows it to effectively coordinate with metals like rhodium or iridium, enhancing the efficiency and selectivity of the cata
This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a chiral ligand in transition metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Its unique structure, featuring biphenyl and bis(4-chlorophenyl)phosphine groups, allows it to effectively coordinate with metals like rhodium or iridium, enhancing the efficiency and selectivity of the catalytic system. Applications include the production of chiral pharmaceuticals, fine chemicals, and agrochemicals, where precise stereocontrol is critical. Its stability and ability to induce high enantiomeric excess make it a valuable tool in advanced organic synthesis.
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...