2,6-Bis[(3aR,8aS)-()-8H-indeno[1,2-d]oxazolin-2-yl)pyridine

98%

Reagent Code: #68289
fingerprint
CAS Number 357209-32-6

science Other reagents with same CAS 357209-32-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.44 g/mol
Formula C₂₅H₁₉N₃O₂
badge Registry Numbers
MDL Number MFCD09265074
inventory_2 Storage & Handling
Storage room temperature

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 the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of transition metal-catalyzed processes. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure compounds, which are essential for developing drugs with specific biological activities. Additionally, it finds use in academic research for exploring new catalytic methodologies and understanding reaction mechanisms.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Tan, Powder or Crystalline Powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿55,980.00
inventory 250mg
10-20 days ฿3,860.00
inventory 1g
10-20 days ฿13,600.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2,6-Bis[(3aR,8aS)-()-8H-indeno[1,2-d]oxazolin-2-yl)pyridine
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 the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of transition metal-catalyzed processes. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure compounds, which are essential for developing drugs with specific biological activiti

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 the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of transition metal-catalyzed processes. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure compounds, which are essential for developing drugs with specific biological activities. Additionally, it finds use in academic research for exploring new catalytic methodologies and understanding reaction mechanisms.

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...