(3aS,3a'S,8aR,8a'R)-2,2'-(1,3-Bis(3,5-di-t-butylphenyl)propane-2,2-diyl)bis(8,8a-dihydro-3aH-indeno[1,2-d]oxazole)

98%

Reagent Code: #55341
fingerprint
CAS Number 1435467-29-0

science Other reagents with same CAS 1435467-29-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 735.0500 g/mol
Formula C₅₁H₆₂N₂O₂
badge Registry Numbers
MDL Number MFCD27978391
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its robust structure and steric properties enhance its performance in metal-catalyzed reactions, such as hydrogenation and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and as a component in chiral catalysts for research and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,617.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3aS,3a'S,8aR,8a'R)-2,2'-(1,3-Bis(3,5-di-t-butylphenyl)propane-2,2-diyl)bis(8,8a-dihydro-3aH-indeno[1,2-d]oxazole)
No image available

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its robust structure and steric properties enhance its performance in metal-catalyzed reactions, such as hydrogenation and carbon-carbon bond formation. Additionally, it is emp

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its robust structure and steric properties enhance its performance in metal-catalyzed reactions, such as hydrogenation and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and as a component in chiral catalysts for research and industrial applications.

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...