(S,S)-4,4'-Diisopropyl-4,5,4',5'-tetrahydro[2.2]bioxazolyl

98%, ee 99%

Reagent Code: #38653
fingerprint
CAS Number 131833-89-1

science Other reagents with same CAS 131833-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.3 g/mol
Formula C₁₂H₂₀N₂O₂
thermostat Physical Properties
Melting Point 58-60 °C
Boiling Point 280.4±23.0 °C
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it finds use in the preparation of fine chemicals and agrochemicals, where precise control over stereochemistry is essential for desired biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500 mg
10-20 days ฿7,090.00
inventory 100 mg
10-20 days ฿1,440.00
inventory 1 g
10-20 days ฿14,150.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S,S)-4,4'-Diisopropyl-4,5,4',5'-tetrahydro[2.2]bioxazolyl
No image available
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additi
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its application is significant in the pharmaceutical industry for the synthesis of enantiomerically pure drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it finds use in the preparation of fine chemicals and agrochemicals, where precise control over stereochemistry is essential for desired biological activity.
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...