(4R,4'R)-2,2'-(Pentane-3,3-diyl)bis(4-benzyl-4,5-dihydrooxazole)

97%

Reagent Code: #69783
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CAS Number 1192345-90-6

science Other reagents with same CAS 1192345-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 390.51 g/mol
Formula C₂₅H₃₀N₂O₂
badge Registry Numbers
MDL Number MFCD31010443
thermostat Physical Properties
Boiling Point 506.6±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its structure, featuring dihydrooxazole rings, makes it effective in coordinating with transition metals, enhancing the selectivity and efficiency of catalytic processes. Applications include the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where high enantiomeric purity is essential. Its use in asymmetric hydrogenation and cyclopropanation reactions is also notable, contributing to the production of complex chiral molecules with high precision.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,267.00

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(4R,4'R)-2,2'-(Pentane-3,3-diyl)bis(4-benzyl-4,5-dihydrooxazole)
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This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its structure, featuring dihydrooxazole rings, makes it effective in coordinating with transition metals, enhancing the selectivity and efficiency of catalytic processes. Applications include the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where hi

This chemical is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its structure, featuring dihydrooxazole rings, makes it effective in coordinating with transition metals, enhancing the selectivity and efficiency of catalytic processes. Applications include the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where high enantiomeric purity is essential. Its use in asymmetric hydrogenation and cyclopropanation reactions is also notable, contributing to the production of complex chiral molecules with high precision.

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