CAS 154026-93-4
:Ácido hexanoico, 6-cloro-3,5-diidroxi-, éster 1,1-dimetiletilo, (3R,5S)-
- tert-butyl (3R,5S)-6-chloro-3,5-dihydroxyhexanoate
Hexanoic acid, 6-chloro-3,5-dihydroxy-, 1,1-dimethylethyl ester, (3R,5S)-
CAS:Fórmula:C10H19ClO4Cor e Forma:LiquidPeso molecular:238.7085(3R,5S)-tert-Butyl 6-chloro-3,5-dihydroxyhexanoate
CAS:(3R,5S)-tert-Butyl 6-chloro-3,5-dihydroxyhexanoate is a secondary metabolite that is used as a lipid-lowering drug. It is synthesized by an asymmetric synthesis of 3,5-dihydroxyhexanoic acid and tertiary butyl alcohol. The synthetic pathway starts with the conversion of diaminopentane phosphate to diaminopentane dihydrogen phosphate in the presence of sodium carbonate. This reaction produces a mixture of (2S,4S)- and (2R,4S) -enantiomers of diaminopentane dihydrogen phosphate. The (2S,4S) -enantiomer is then converted to (2R,4S) -enantiomer by dehydrogenase enzymes. Hydroxylation of the (2R,4S) -enantiomer occurs with the help of a lipase enzyme
Fórmula:C10H19ClO4Pureza:Min. 95%Peso molecular:238.71 g/mol1,1-Dimethylethyl (3R,5S)-6-Chloro-3,5-dihydroxyhexanoate
CAS:Produto ControladoStability Hygroscopic
Applications (3R,5S)-6-Chloro-3,5-dihydroxyhexanoic Acid tert-Butyl Ester is an intermediate in the synthesis of Rosuvastatin (R700500), a selective, competitive HMG-CoA reductase inhibitor.
References Amidjojo, M., et al.: App. Microbiol. Biotechol., 69, 9 (2005);Fórmula:C10H19ClO4Pureza:~90%Cor e Forma:NeatPeso molecular:238.71




