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Home  > N,N'-(1S,2S)-1,2-Cyclohexanediylbis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea

AA13482

1140969-69-2 | N,N'-(1S,2S)-1,2-Cyclohexanediylbis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $27.00 $19.00 -   +
250mg 95% in stock $63.00 $45.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA13482
Chemical Name: N,N'-(1S,2S)-1,2-Cyclohexanediylbis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea
CAS Number: 1140969-69-2
Molecular Formula: C24H20F12N4S2
Molecular Weight: 656.5532
MDL Number: MFCD23160163
SMILES: S=C(Nc1cc(cc(c1)C(F)(F)F)C(F)(F)F)N[C@H]1CCCC[C@@H]1NC(=S)Nc1cc(cc(c1)C(F)(F)F)C(F)(F)F

 

Upstream Synthesis Route
  • The compound N,N'-(1S,2S)-1,2-Cyclohexanediylbis[N'-[3,5-bis(trifluoromethyl)phenyl]thiourea], $name$, is a versatile reagent widely used in chemical synthesis. Its unique structure provides a chiral environment for various reactions, making it particularly useful in asymmetric synthesis. $name$ can effectively catalyze a range of transformations, such as asymmetric hydrogenation, reductive amination, and carbon-carbon bond formation. Its ability to control the stereochemistry of products makes it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, $name$ has shown promising results in the construction of complex molecular structures with high enantioselectivity. Its application extends to the development of new methodologies in organic chemistry, driving innovation in the field of chemical synthesis.
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