N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(9R)-6'-methoxycinchonan-9-yl]thiourea

≥98%,99%d.e.

Reagent Code: #57519
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CAS Number 852913-25-8

science Other reagents with same CAS 852913-25-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 594.6 g/mol
Formula C₂₉H₂₈F₆N₄OS
thermostat Physical Properties
Melting Point 150°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of optically active compounds with high selectivity. Its application is significant in pharmaceutical synthesis, where it aids in producing chiral intermediates for drugs. Additionally, it is employed in organic synthesis to facilitate transformations such as Michael additions, Mannich reactions, and other carbon-carbon bond-forming processes. Its unique structure, featuring trifluoromethyl groups and a cinchona alkaloid derivative, enhances its catalytic efficiency and stereocontrol, making it valuable in the development of complex organic molecules.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿4,446.00
inventory 100mg
10-20 days ฿9,297.00
inventory 500mg
10-20 days ฿30,150.00

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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(9R)-6'-methoxycinchonan-9-yl]thiourea
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This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of optically active compounds with high selectivity. Its application is significant in pharmaceutical synthesis, where it aids in producing chiral intermediates for drugs. Additionally, it is employed in organic synthesis to facilitate transformations such as Michael additions, Mannich reactions, and other carbon-carbon bond-forming proce

This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of optically active compounds with high selectivity. Its application is significant in pharmaceutical synthesis, where it aids in producing chiral intermediates for drugs. Additionally, it is employed in organic synthesis to facilitate transformations such as Michael additions, Mannich reactions, and other carbon-carbon bond-forming processes. Its unique structure, featuring trifluoromethyl groups and a cinchona alkaloid derivative, enhances its catalytic efficiency and stereocontrol, making it valuable in the development of complex organic molecules.

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