The molecule features a biphenyl aromatic core, a single defined stereocenter (1R), and a hydroxymethyl functional group, enabling further chemical derivatization while maintaining stereochemical integrity. The tert-butyl (Boc) protecting group provides stability during multistep synthesis and can be selectively removed under mild acidic conditions. This compound has no direct therapeutic application and is intended strictly for research and intermediate use. Carbamic acid, N-((1R)-2-(1,1′-biphenyl)-4-yl-1-(hydroxymethyl)ethyl)-, 1,1-dimethylethyl ester is a chiral Boc-protected carbamate used as a synthetic intermediate in pharmaceutical and fine chemical research.
Carbamic acid, N-((1R)-2-(1,1′-biphenyl)-4-YL-1-(hydroxymethyl)ethyl)-, 1,1-dimethylethyl ester
| API Name | Sacubitril |
|---|---|
| CAS No | 1426129-50-1 |
| Molecular Formula | C20H25NO3 |
| Molecular Weight | 327.4 g/mol |
| Synonyms | tert-butyl N-[(2R)-1-hydroxy-3-(4-phenylphenyl)propan-2-yl]carbamate |
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