(4S,4'S)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)

97%

Reagent Code: #36985
fingerprint
CAS Number 2172801-78-2

science Other reagents with same CAS 2172801-78-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 626.8693 g/mol
Formula C₄₃H₅₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its structure, featuring oxazoline rings and bulky tert-butyl groups, enhances its ability to induce asymmetry in reactions. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where specific stereochemistry is required. Additionally, its stability and efficiency in catalytic systems contribute to its widespread use in academic and industrial research for developing enantioselective methodologies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,726.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4S,4'S)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its structure, featuring oxazoline rings and bulky tert-butyl groups, enhances its ability to induce asymmetry in reactions. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine che

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its structure, featuring oxazoline rings and bulky tert-butyl groups, enhances its ability to induce asymmetry in reactions. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where specific stereochemistry is required. Additionally, its stability and efficiency in catalytic systems contribute to its widespread use in academic and industrial research for developing enantioselective methodologies.

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...