(4R,4'R,5S,5'S)-2,2'-cyclopropylidenebis[4,5-dihydro-4,5-diphenyl-Oxazole

98%

Reagent Code: #59713
fingerprint
CAS Number 229184-96-7

science Other reagents with same CAS 229184-96-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 484.59 g/mol
Formula C₃₃H₂₈N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring a cyclopropylidene bridge and diphenyloxazole moieties, makes it highly effective in enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in organic synthesis to produce chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its rigid framework and stereochemical control contribute to high selectivity and yield in catalytic processes, making it a valuable tool in the development of optically active compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,195.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4R,4'R,5S,5'S)-2,2'-cyclopropylidenebis[4,5-dihydro-4,5-diphenyl-Oxazole
No image available

This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring a cyclopropylidene bridge and diphenyloxazole moieties, makes it highly effective in enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in organic synthesis to produce chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its rigid framework and stereochemical control contr

This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring a cyclopropylidene bridge and diphenyloxazole moieties, makes it highly effective in enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in organic synthesis to produce chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its rigid framework and stereochemical control contribute to high selectivity and yield in catalytic processes, making it a valuable tool in the development of optically active 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...