(R)-(6,6'-Dimethoxybiphenyl-2,2'-diyl)bis(di-2-furylphosphine)

98%

Reagent Code: #68643
fingerprint
CAS Number 145214-57-9

science Other reagents with same CAS 145214-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 542.45 g/mol
Formula C₃₀H₂₄O₆P₂
badge Registry Numbers
MDL Number MFCD09753004
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical precision. The compound's structure, featuring dimethoxybiphenyl and di-2-furylphosphine groups, enhances its ability to induce chirality in catalytic processes, making it valuable for reactions like hydrogenation, cross-coupling, and allylic substitution. Its use contributes to the development of more efficient and selective synthetic routes for complex organic molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,399.00
inventory 1g
10-20 days ฿37,431.00
inventory 250mg
10-20 days ฿12,042.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-(6,6'-Dimethoxybiphenyl-2,2'-diyl)bis(di-2-furylphosphine)
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical precision. The compound's structure, featuring dimethoxybiphenyl and di-2-furylphosphine groups, enhances its ability to induce chirality in catalytic processes, making it valuable for reactions li

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical precision. The compound's structure, featuring dimethoxybiphenyl and di-2-furylphosphine groups, enhances its ability to induce chirality in catalytic processes, making it valuable for reactions like hydrogenation, cross-coupling, and allylic substitution. Its use contributes to the development of more efficient and selective synthetic routes for complex organic molecules.

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...