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

97%

Reagent Code: #59737
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CAS Number 298693-03-5

science Other reagents with same CAS 298693-03-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.47 g/mol
Formula C₁₉H₃₂N₂O₂
badge Registry Numbers
MDL Number MFCD32201206
thermostat Physical Properties
Melting Point 51.0-52.0 °C
Boiling Point 125-130 °C(Press: 0.4 Torr)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating the formation of chiral centers in organic molecules, which is essential for producing pharmaceuticals, agrochemicals, and fine chemicals with high enantiomeric purity. Its unique structure allows it to effectively coordinate with transition metals, such as rhodium or iridium, to form catalysts that drive asymmetric hydrogenation, cyclization, and other stereospecific reactions. This makes it valuable in industries where precise control over molecular chirality is critical for the efficacy and safety of the final product.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,159.00

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(4S,4'S)-2,2'-(Cyclopentane-1,1-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating the formation of chiral centers in organic molecules, which is essential for producing pharmaceuticals, agrochemicals, and fine chemicals with high enantiomeric purity. Its unique structure allows it to effectively coordinate with transition metals, such as rhodium or iridium, to form catalysts that drive asymmetric hydrogenation, cyclization,

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating the formation of chiral centers in organic molecules, which is essential for producing pharmaceuticals, agrochemicals, and fine chemicals with high enantiomeric purity. Its unique structure allows it to effectively coordinate with transition metals, such as rhodium or iridium, to form catalysts that drive asymmetric hydrogenation, cyclization, and other stereospecific reactions. This makes it valuable in industries where precise control over molecular chirality is critical for the efficacy and safety of the final product.

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