![(R)-3-(4-Cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropionamide (CAS 1132656-73-5) - chemical str](https://media.scbt.com/product/r-3-4-cyanophenoxy-n-4-cyano-3-trifluoromethyl-phenyl-2-hydroxy-2-methylpropionamide-1132656-73-5-structure_40_73_b_407318.jpg)
![Molecular structure of (R)-3-(4-Cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropionamide, CAS Number: 1132656-73-5 (R)-3-(4-Cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropionamide (CAS 1132656-73-5) - chemical str](https://media.scbt.com/product/r-3-4-cyanophenoxy-n-4-cyano-3-trifluoromethyl-phenyl-2-hydroxy-2-methylpropionamide-1132656-73-5-structure_40_73_t_407318.jpg)
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(R)-3-(4-Cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropionamide is a compound that is of particular interest in the field of organic and medicinal chemistry research. This compound, with its multiple functional groups including cyano groups, a trifluoromethyl group, and a hydroxy-methylpropionamide moiety, presents a complex structure that allows for the exploration of various chemical interactions and binding affinities. It is often utilized as a ligand in the study of enzyme inhibition, where it can interact with specific active sites to elucidate enzyme function and regulation. Moreover, the stereospecificity indicated by the (R)-configuration adds an additional layer of complexity, making it a useful chiral compound for the study of enantioselective reactions and for understanding the role of chirality in molecular recognition processes. The compound′s unique structural features also make it a candidate for the design of new molecules with potential applications in chemical synthesis and industry.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(R)-3-(4-Cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropionamide, 25 mg | sc-478400 | 25 mg | $600.00 |