(11bS)-2,6-Bis[4-(1,1-dimethylethyl)phenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin

≥98%,99%e.e.

Reagent Code: #70510
fingerprint
CAS Number 1217901-32-0

science Other reagents with same CAS 1217901-32-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 612.7 g/mol
Formula C₄₀H₃₇O₄P
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to coordinate with transition metals, forming complexes that are highly effective in enantioselective hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. This makes it valuable in the production of pharmaceuticals, where the correct stereochemistry of a drug molecule is essential for its efficacy and safety. Additionally, its stability and selectivity make it a preferred choice in fine chemical synthesis, enabling the creation of complex molecules with high precision.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿24,210.00
inventory 100mg
10-20 days ฿3,231.00
inventory 250mg
10-20 days ฿6,651.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(11bS)-2,6-Bis[4-(1,1-dimethylethyl)phenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
No image available

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to coordinate with transition metals, forming complexes that are highly effective in enantioselective hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. This makes it valuable in the production of pharmaceuticals, where the correct stereochemistry of a drug molecule is essential for its e

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to coordinate with transition metals, forming complexes that are highly effective in enantioselective hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. This makes it valuable in the production of pharmaceuticals, where the correct stereochemistry of a drug molecule is essential for its efficacy and safety. Additionally, its stability and selectivity make it a preferred choice in fine chemical synthesis, enabling the creation of complex molecules with high precision.

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...