Bis(2-((S)-4-Phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine

97%

Reagent Code: #55692
fingerprint
CAS Number 485394-21-6

science Other reagents with same CAS 485394-21-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 459.5384 g/mol
Formula C₃₀H₂₅N₃O₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of asymmetric catalysis, where it serves as a chiral ligand in various organic synthesis processes. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing chiral molecules with high optical purity. These reactions are widely applied in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) that require specific stereochemistry to achieve desired biological activity. Additionally, it finds use in academic research for developing new methodologies in asymmetric synthesis, contributing to advancements in synthetic organic chemistry. Its robust structure and chiral properties make it a valuable tool for chemists aiming to create complex, enantiomerically pure compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,580.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Bis(2-((S)-4-Phenyl-4,5-dihydrooxazol-2-yl)phenyl)amine
No image available

This chemical is primarily utilized in the field of asymmetric catalysis, where it serves as a chiral ligand in various organic synthesis processes. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing chiral molecules with high optical purity. These reactions are widely applied in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) that require specific stereochemistry to achieve desired biological activity. Additi

This chemical is primarily utilized in the field of asymmetric catalysis, where it serves as a chiral ligand in various organic synthesis processes. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing chiral molecules with high optical purity. These reactions are widely applied in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) that require specific stereochemistry to achieve desired biological activity. Additionally, it finds use in academic research for developing new methodologies in asymmetric synthesis, contributing to advancements in synthetic organic chemistry. Its robust structure and chiral properties make it a valuable tool for chemists aiming to create complex, enantiomerically pure compounds.

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...