N-[(1R,2R)-2-[Bis(phenylmethyl)amino]cyclohexyl]-N'-[3,5-bis(trifluoromethyl)phenyl]thiourea

≥98%,99%e.e.

Reagent Code: #70684
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CAS Number 1240466-16-3

science Other reagents with same CAS 1240466-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 565.6 g/mol
Formula C₂₉H₂₉F₆N₃S
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of organic chemistry as a chiral catalyst or ligand in asymmetric synthesis. Its unique structure, featuring a thiourea moiety and trifluoromethyl groups, makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is essential. Additionally, its ability to act as a hydrogen bond donor enhances its utility in molecular recognition and supramolecular chemistry applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,210.00

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N-[(1R,2R)-2-[Bis(phenylmethyl)amino]cyclohexyl]-N'-[3,5-bis(trifluoromethyl)phenyl]thiourea
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This compound is primarily utilized in the field of organic chemistry as a chiral catalyst or ligand in asymmetric synthesis. Its unique structure, featuring a thiourea moiety and trifluoromethyl groups, makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is essential. Additionally, its ability to act as a

This compound is primarily utilized in the field of organic chemistry as a chiral catalyst or ligand in asymmetric synthesis. Its unique structure, featuring a thiourea moiety and trifluoromethyl groups, makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is essential. Additionally, its ability to act as a hydrogen bond donor enhances its utility in molecular recognition and supramolecular chemistry applications.

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