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

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Reagent Code: #62517
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CAS Number 1649427-16-6

science Other reagents with same CAS 1649427-16-6

blur_circular Chemical Specifications

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Weight 583.59 g/mol
Formula C₃₁H₂₃F₆N₃S
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized as a chiral catalyst or ligand in asymmetric synthesis, particularly in organic transformations where enantioselectivity is crucial. It is often employed in the development of pharmaceuticals, where the production of specific enantiomers is essential for drug efficacy and safety. Its unique structure allows it to effectively induce chirality in reactions such as hydrogenations, cycloadditions, and other carbon-carbon bond-forming processes. Additionally, it finds application in academic research for studying enantioselective mechanisms and developing novel catalytic methods. Its trifluoromethyl groups enhance its stability and reactivity, making it a valuable tool in synthetic organic chemistry.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,001.00

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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(S)-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 organic transformations where enantioselectivity is crucial. It is often employed in the development of pharmaceuticals, where the production of specific enantiomers is essential for drug efficacy and safety. Its unique structure allows it to effectively induce chirality in reactions such as hydrogenations, cycloadditions, and other carbon-carbon bond-forming processes. Additionally, it finds appli

This compound is primarily utilized as a chiral catalyst or ligand in asymmetric synthesis, particularly in organic transformations where enantioselectivity is crucial. It is often employed in the development of pharmaceuticals, where the production of specific enantiomers is essential for drug efficacy and safety. Its unique structure allows it to effectively induce chirality in reactions such as hydrogenations, cycloadditions, and other carbon-carbon bond-forming processes. Additionally, it finds application in academic research for studying enantioselective mechanisms and developing novel catalytic methods. Its trifluoromethyl groups enhance its stability and reactivity, making it a valuable tool in synthetic organic chemistry.

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