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

≥98%,99%e.e.

Reagent Code: #70712
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CAS Number 1233369-39-5

science Other reagents with same CAS 1233369-39-5

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 organic synthesis and catalysis, particularly in asymmetric transformations. It serves as a chiral catalyst or ligand in various enantioselective reactions, enabling the production of optically active compounds with high selectivity. Its structure, featuring a thiourea moiety and trifluoromethyl groups, makes it effective in hydrogen bonding interactions, which are crucial for stabilizing transition states in catalytic processes. It is often employed in the synthesis of pharmaceuticals and fine chemicals where precise stereochemistry is essential. Additionally, its robust design allows for use in challenging reaction conditions, making it a valuable tool in advanced synthetic chemistry.

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inventory 100mg
10-20 days ฿16,938.00

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N-[(1S,2S)-2-[Bis(phenylmethyl)amino]cyclohexyl]-N'-[3,5-bis(trifluoromethyl)phenyl]thiourea
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This compound is primarily utilized in organic synthesis and catalysis, particularly in asymmetric transformations. It serves as a chiral catalyst or ligand in various enantioselective reactions, enabling the production of optically active compounds with high selectivity. Its structure, featuring a thiourea moiety and trifluoromethyl groups, makes it effective in hydrogen bonding interactions, which are crucial for stabilizing transition states in catalytic processes. It is often employed in the synthesi

This compound is primarily utilized in organic synthesis and catalysis, particularly in asymmetric transformations. It serves as a chiral catalyst or ligand in various enantioselective reactions, enabling the production of optically active compounds with high selectivity. Its structure, featuring a thiourea moiety and trifluoromethyl groups, makes it effective in hydrogen bonding interactions, which are crucial for stabilizing transition states in catalytic processes. It is often employed in the synthesis of pharmaceuticals and fine chemicals where precise stereochemistry is essential. Additionally, its robust design allows for use in challenging reaction conditions, making it a valuable tool in advanced synthetic chemistry.

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