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Home  > (S)-1-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine fumarate

AA52958

1214741-14-6 | (S)-1-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine fumarate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% 2 weeks $35.00 $25.00 -   +
250mg 97% 2 weeks $50.00 $35.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA52958
Chemical Name: (S)-1-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine fumarate
CAS Number: 1214741-14-6
Molecular Formula: C24H23F6NO5
Molecular Weight: 519.4335
MDL Number: MFCD29059866
SMILES: OC(=O)C=CC(=O)O.C=C[C@](c1ccccc1)(CO[C@@H](c1cc(cc(c1)C(F)(F)F)C(F)(F)F)C)N

 

Upstream Synthesis Route
  • (S)-1-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine fumarate is a valuable compound used in chemical synthesis as a versatile chiral building block. Due to its specific stereochemistry, this compound plays a crucial role in asymmetric synthesis, allowing chemists to control the chirality of the final products.In chemical synthesis, this compound serves as a key intermediate for the preparation of various chiral molecules with precise stereochemistry. Its unique structure containing both an amine group and a double bond makes it a valuable starting material for the synthesis of complex pharmaceuticals, agrochemicals, and functional materials.By incorporating (S)-1-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine fumarate into synthesis routes, chemists can efficiently access enantiopure compounds, essential in the production of drugs with enhanced therapeutic effects and reduced side effects. Its application extends to the development of novel catalysts, ligands, and other biologically active molecules.Overall, (S)-1-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine fumarate is a valuable tool in the hands of synthetic chemists, enabling precise control over stereochemistry and facilitating the creation of diverse chiral compounds with applications across various industries.
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