(4S,4'S)-4,4'-Bis(1,1-dimethylethyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole

97%

Reagent Code: #69788
fingerprint
CAS Number 135565-31-0

science Other reagents with same CAS 135565-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.35 g/mol
Formula C₁₄H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD32671514
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to the development of catalysts for hydrogenation and carbon-carbon bond formation, enhancing the efficiency and selectivity of these processes. Additionally, it is employed in the synthesis of complex natural products and bioactive compounds, contributing to advancements in medicinal chemistry and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,412.00
inventory 250mg
10-20 days ฿4,968.00
inventory 1g
10-20 days ฿16,731.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4S,4'S)-4,4'-Bis(1,1-dimethylethyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole
No image available

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to the development of catalysts for hydrogenation and carbon-carbon bond formation, enhancing the efficiency and selectivity of these processes. Additionally, it is employed in the synthesis of complex

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to the development of catalysts for hydrogenation and carbon-carbon bond formation, enhancing the efficiency and selectivity of these processes. Additionally, it is employed in the synthesis of complex natural products and bioactive compounds, contributing to advancements in medicinal chemistry and drug discovery.

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...