(S)-4-Benzyl-2-((S)-7'-(bis(3,5-dimethylphenyl)phosphino)-2,2',3,3'-tetrahydro-1,1'-spirobi[inden]-7-yl)-4,5-dihydrooxazole

98%

Reagent Code: #59715
fingerprint
CAS Number 913829-90-0

science Other reagents with same CAS 913829-90-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 619.77 g/mol
Formula C₄₃H₄₂NOP
badge Registry Numbers
MDL Number MFCD21362522
thermostat Physical Properties
Boiling Point 755.2±60.0 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its unique structure, featuring a spirobi[inden] core and a phosphine group, enhances its ability to induce high enantioselectivity and reactivity in catalytic processes. This makes it valuable in the synthesis of pharmaceuticals, fine chemicals, and other complex organic molecules where precise stereochemical control is essential. Additionally, its application extends to the development of advanced materials and agrochemicals, where asymmetric synthesis is increasingly important.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,375.00
inventory 10mg
10-20 days ฿3,096.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-4-Benzyl-2-((S)-7'-(bis(3,5-dimethylphenyl)phosphino)-2,2',3,3'-tetrahydro-1,1'-spirobi[inden]-7-yl)-4,5-dihydrooxazole
No image available

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its unique structure, featuring a spirobi[inden] core and a phosphine group, enhances its ability to induce high enantioselectivity and reactivity in catalytic processes. This makes it valuable in the synthesis of ph

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its unique structure, featuring a spirobi[inden] core and a phosphine group, enhances its ability to induce high enantioselectivity and reactivity in catalytic processes. This makes it valuable in the synthesis of pharmaceuticals, fine chemicals, and other complex organic molecules where precise stereochemical control is essential. Additionally, its application extends to the development of advanced materials and agrochemicals, where asymmetric synthesis is increasingly important.

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...