1-(3,5-Bis(trifluoromethyl)phenyl)-3-((1R,2R)-2-(dipentylamino)cyclohexyl)thiourea

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Reagent Code: #70576
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CAS Number 2097443-87-1

science Other reagents with same CAS 2097443-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 525.64 g/mol
Formula C₂₅H₃₇F₆N₃S
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This chemical is primarily used in the field of organic synthesis and medicinal chemistry due to its unique structural properties. It serves as a key intermediate in the development of pharmaceutical compounds, particularly those targeting specific receptors or enzymes. Its trifluoromethyl groups enhance its binding affinity and metabolic stability, making it valuable in drug discovery. Additionally, the thiourea moiety and chiral cyclohexyl structure contribute to its use in asymmetric catalysis, aiding in the synthesis of enantiomerically pure compounds. Its application extends to research in biochemistry, where it is studied for its potential in modulating biological pathways or as a tool compound in mechanistic studies.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,482.00

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1-(3,5-Bis(trifluoromethyl)phenyl)-3-((1R,2R)-2-(dipentylamino)cyclohexyl)thiourea
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This chemical is primarily used in the field of organic synthesis and medicinal chemistry due to its unique structural properties. It serves as a key intermediate in the development of pharmaceutical compounds, particularly those targeting specific receptors or enzymes. Its trifluoromethyl groups enhance its binding affinity and metabolic stability, making it valuable in drug discovery. Additionally, the thiourea moiety and chiral cyclohexyl structure contribute to its use in asymmetric catalysis, aiding

This chemical is primarily used in the field of organic synthesis and medicinal chemistry due to its unique structural properties. It serves as a key intermediate in the development of pharmaceutical compounds, particularly those targeting specific receptors or enzymes. Its trifluoromethyl groups enhance its binding affinity and metabolic stability, making it valuable in drug discovery. Additionally, the thiourea moiety and chiral cyclohexyl structure contribute to its use in asymmetric catalysis, aiding in the synthesis of enantiomerically pure compounds. Its application extends to research in biochemistry, where it is studied for its potential in modulating biological pathways or as a tool compound in mechanistic studies.

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