(4R,4'R)-2,2'-(Heptane-4,4-diyl)bis(4-phenyl-4,5-dihydrooxazole)

95%

Reagent Code: #231345
fingerprint
CAS Number 2447575-76-8

science Other reagents with same CAS 2447575-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 390.52 g/mol
Formula C₂₅H₃₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid bis(oxazoline) structure enables effective stereocontrol in reactions such as cyclopropanations, Diels-Alder, and aldol reactions when coordinated with metal centers like copper or nickel. The heptane backbone with defined stereochemistry enhances selectivity and stability in catalytic systems. Commonly employed in pharmaceutical synthesis where high enantiomeric purity is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,690.00
250mg
10-20 days ฿6,250.00
1g
10-20 days ฿18,010.00
(4R,4'R)-2,2'-(Heptane-4,4-diyl)bis(4-phenyl-4,5-dihydrooxazole)
No image available

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid bis(oxazoline) structure enables effective stereocontrol in reactions such as cyclopropanations, Diels-Alder, and aldol reactions when coordinated with metal centers like copper or nickel. The heptane backbone with defined stereochemistry enhances selectivity and stability in catalytic systems. Commonly employed in pharmaceutical synthesis where high enantiomeric purity is required.

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid bis(oxazoline) structure enables effective stereocontrol in reactions such as cyclopropanations, Diels-Alder, and aldol reactions when coordinated with metal centers like copper or nickel. The heptane backbone with defined stereochemistry enhances selectivity and stability in catalytic systems. Commonly employed in pharmaceutical synthesis where high enantiomeric purity is required.

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...