N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(R)-2'-(dimethylamino)[1,1'-binaphthalen]-2-yl]thiourea

≥98%,99%e.e.

Reagent Code: #57499
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CAS Number 866940-63-8

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Weight 583.6 g/mol
Formula C₃₁H₂₃F₆N₃S
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective reactions. Its unique structure, featuring trifluoromethyl groups and a binaphthyl backbone, enhances its ability to induce chirality in various organic transformations. It is often employed in the synthesis of pharmaceuticals, where the production of single enantiomers is crucial for drug efficacy and safety. Additionally, it finds application in the development of advanced materials and fine chemicals, where precise control over molecular configuration is required. Its thiourea moiety also makes it effective in hydrogen-bonding catalysis, facilitating reactions such as Michael additions and aldol condensations.

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inventory 100mg
10-20 days ฿9,837.00

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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(R)-2'-(dimethylamino)[1,1'-binaphthalen]-2-yl]thiourea
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This compound is primarily utilized as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective reactions. Its unique structure, featuring trifluoromethyl groups and a binaphthyl backbone, enhances its ability to induce chirality in various organic transformations. It is often employed in the synthesis of pharmaceuticals, where the production of single enantiomers is crucial for drug efficacy and safety. Additionally, it finds application in the development of advanced materi

This compound is primarily utilized as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective reactions. Its unique structure, featuring trifluoromethyl groups and a binaphthyl backbone, enhances its ability to induce chirality in various organic transformations. It is often employed in the synthesis of pharmaceuticals, where the production of single enantiomers is crucial for drug efficacy and safety. Additionally, it finds application in the development of advanced materials and fine chemicals, where precise control over molecular configuration is required. Its thiourea moiety also makes it effective in hydrogen-bonding catalysis, facilitating reactions such as Michael additions and aldol condensations.

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