(4S)-4-Tert-butyl-2-[1-[(4S)-4-tert-butyl-4,5-dihydro-1,3-oxazol-2-yl]cyclopropyl]-4,5-dihydro-1,3-oxazole

98%

Reagent Code: #59733
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CAS Number 195379-09-0

science Other reagents with same CAS 195379-09-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.41642 g/mol
Formula C₁₇H₂₈N₂O₂
thermostat Physical Properties
Melting Point 79.0-80.0 °C
Boiling Point 125-130 °C(Press: 0.4 Torr)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral auxiliary or ligand in asymmetric catalysis. Its unique structure, featuring oxazole rings and cyclopropyl groups, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, where precise stereochemical outcomes are crucial for the biological activity of the final product. Additionally, it finds use in the development of advanced materials, where its rigid and sterically hindered structure can influence the properties of polymers or coordination complexes. Its application is also seen in academic research for exploring novel catalytic processes and reaction mechanisms.

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Test Parameter Specification
APPEARANCE White to Light yellow to Yellow Solid
Purity (%) 97.5-100
Specific Rotation [A]20/D (C=1.1 In CHCl3)(deg) -83--90
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿7,182.00
inventory 50mg
10-20 days ฿28,530.00

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(4S)-4-Tert-butyl-2-[1-[(4S)-4-tert-butyl-4,5-dihydro-1,3-oxazol-2-yl]cyclopropyl]-4,5-dihydro-1,3-oxazole
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This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral auxiliary or ligand in asymmetric catalysis. Its unique structure, featuring oxazole rings and cyclopropyl groups, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, where precise stereochemical outcomes are crucial for the biological activity of the final product. Additionally, it finds use in the development o

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral auxiliary or ligand in asymmetric catalysis. Its unique structure, featuring oxazole rings and cyclopropyl groups, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, where precise stereochemical outcomes are crucial for the biological activity of the final product. Additionally, it finds use in the development of advanced materials, where its rigid and sterically hindered structure can influence the properties of polymers or coordination complexes. Its application is also seen in academic research for exploring novel catalytic processes and reaction mechanisms.

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