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

97%

Reagent Code: #59735
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CAS Number 298693-04-6

science Other reagents with same CAS 298693-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.50 g/mol
Formula C₂₀H₃₄N₂O₂
badge Registry Numbers
MDL Number MFCD32201212
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The compound’s stability and efficiency in creating chiral environments make it a preferred choice for researchers developing advanced synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,546.00

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(4S,4'S)-2,2'-(Cyclohexane-1,1-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The compound’s stability and efficiency in creating chiral envi

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The compound’s stability and efficiency in creating chiral environments make it a preferred choice for researchers developing advanced synthetic methodologies.

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