(4S,4'S)-2,2'-[2-phenyl-1-(phenylmethyl)ethylidene]bis[4,5-dihydro-4-phenyl-Oxazole

98%, ee 99%

Reagent Code: #36980
fingerprint
CAS Number 319489-87-7

science Other reagents with same CAS 319489-87-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.6 g/mol
Formula C₃₃H₃₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring oxazole rings and phenyl groups, makes it effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound is often employed in catalytic processes such as hydrogenation, where it helps in achieving high enantiomeric purity of the final product. Additionally, its application extends to organic synthesis, where it serves as a key intermediate in the construction of complex molecules with specific stereochemical configurations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250 mg
10-20 days ฿4,010.00
inventory 25 mg
10-20 days ฿1,430.00
inventory 5 mg
10-20 days ฿790.00
inventory 100 mg
10-20 days ฿1,790.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4S,4'S)-2,2'-[2-phenyl-1-(phenylmethyl)ethylidene]bis[4,5-dihydro-4-phenyl-Oxazole
No image available

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring oxazole rings and phenyl groups, makes it effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound is often employed in catalytic processes such as hydrogenation, where it helps in achieving high enantiomeric purity of the

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring oxazole rings and phenyl groups, makes it effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound is often employed in catalytic processes such as hydrogenation, where it helps in achieving high enantiomeric purity of the final product. Additionally, its application extends to organic synthesis, where it serves as a key intermediate in the construction of complex molecules with specific stereochemical configurations.

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...