
CAS 154026-93-4: Hexanoic acid, 6-chloro-3,5-dihydroxy-, 1,1-dimethylethyl ester, (3R,5S)-
Formula:C10H19ClO4
InChI:InChI=1/C10H19ClO4/c1-10(2,3)15-9(14)5-7(12)4-8(13)6-11/h7-8,12-13H,4-6H2,1-3H3/t7-,8+/m1/s1
Synonyms:- tert-butyl (3R,5S)-6-chloro-3,5-dihydroxyhexanoate
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Found 6 products.
(3R,5S)-6-Chloro-3,5-dihydroxyhexanoic Acid tert-Butyl Ester (~90%)
CAS:Controlled ProductStability 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);Formula:C10H19ClO4Purity:~90%Color and Shape:NeatMolecular weight:238.71tert-butyl (3R,5S)-6-chloro-3,5-dihydroxyhexanoate
CAS:Formula:C10H19ClO4Color and Shape:LiquidMolecular weight: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 enzymeFormula:C10H19ClO4Purity:Min. 95%Molecular weight:238.71 g/mol