N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(1S,2S)-2-[(11bS)-3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]-1,2-diphenylethyl]thiourea

≥98%,≥99%e.e.

Reagent Code: #57495

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 761.8 g/mol
Formula C₄₅H₃₃F₆N₃S
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of asymmetric catalysis, particularly in enantioselective synthesis. It serves as a chiral catalyst or ligand in various organic reactions, enabling the production of enantiomerically pure compounds. Its application is especially significant in the pharmaceutical industry, where it aids in the synthesis of chiral drug intermediates, ensuring high stereochemical control. Additionally, it is employed in academic research to study and develop new catalytic methodologies for complex organic transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿29,961.00

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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(1S,2S)-2-[(11bS)-3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]-1,2-diphenylethyl]thiourea
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This compound is primarily utilized in the field of asymmetric catalysis, particularly in enantioselective synthesis. It serves as a chiral catalyst or ligand in various organic reactions, enabling the production of enantiomerically pure compounds. Its application is especially significant in the pharmaceutical industry, where it aids in the synthesis of chiral drug intermediates, ensuring high stereochemical control. Additionally, it is employed in academic research to study and develop new catalytic me

This compound is primarily utilized in the field of asymmetric catalysis, particularly in enantioselective synthesis. It serves as a chiral catalyst or ligand in various organic reactions, enabling the production of enantiomerically pure compounds. Its application is especially significant in the pharmaceutical industry, where it aids in the synthesis of chiral drug intermediates, ensuring high stereochemical control. Additionally, it is employed in academic research to study and develop new catalytic methodologies for complex organic transformations.

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