(4S,4'S)-2,2'-(Cyclopentane-1,1-diyl)-bis(4-isopropyl-4,5-dihydrooxazole)

98%

Reagent Code: #59722
fingerprint
CAS Number 1379452-52-4

science Other reagents with same CAS 1379452-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.42 g/mol
Formula C₁₇H₂₈N₂O₂
badge Registry Numbers
MDL Number MFCD24849484
thermostat Physical Properties
Boiling Point 375.7±25.0 °C
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3
Storage 2-8°C

description Product Description

This chemical 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 rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry, where the synthesis of enantiomerically pure drugs is essential for efficacy and safety. Additionally, it finds applications in the development of advanced materials and fine chemicals, where precise stereocontrol is required.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,980.00
inventory 100mg
10-20 days ฿3,060.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4S,4'S)-2,2'-(Cyclopentane-1,1-diyl)-bis(4-isopropyl-4,5-dihydrooxazole)
No image available
This chemical 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 rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical
This chemical 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 rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry, where the synthesis of enantiomerically pure drugs is essential for efficacy and safety. Additionally, it finds applications in the development of advanced materials and fine chemicals, where precise stereocontrol 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...