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CAS 154026-92-3

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TERT-BUTYL (S)-6-CHLORO-5-HYDROXY-3-OXOHEXANOATE

Description:
TERT-BUTYL (S)-6-CHLORO-5-HYDROXY-3-OXOHEXANOATE is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a tert-butyl group, which contributes to its hydrophobic characteristics and steric bulk, influencing its reactivity and solubility. The presence of a chlorine atom at the 6-position and a hydroxyl group at the 5-position on the hexanoate chain indicates that it has potential for various chemical reactions, including nucleophilic substitutions and esterification. The keto group at the 3-position suggests that it may participate in reactions typical of carbonyl compounds, such as aldol condensation. This compound is likely to be a chiral molecule due to the presence of the (S)-configuration, which can have implications in biological activity and pharmacology. Overall, TERT-BUTYL (S)-6-CHLORO-5-HYDROXY-3-OXOHEXANOATE is a versatile compound with potential applications in organic synthesis and medicinal chemistry.
Formula:C10H17ClO4
Synonyms:
  • Tert-Butyl 6-chloro-5(S)-hydroxy-3-oxohexanoate
  • (S)-6-chloro-5-hydroxy-3-oxo-hexanoic acid t-butylester
  • Hexahydro-2(S)-methyl-4-(t-butoxycarboxyl)-1,4-diazepine
  • (S)-tert-butyl 3-methyl-1,4-diazepane-1-carboxylate
  • tert-butyl (S)-3-methyl-1,4-diazepane-1-carboxylate
  • tert-butyl (5S)-6-chloro-5-hydroxy-3-oxohexanoate
  • Hexanoic acid, 6-chloro-5-hydroxy-3-oxo-, 1,1-dimethylethyl ester, (5S)-
  • Rosuvastatin Impurity 83
  • (S)-tert-Butyl 6-chloro-5-hydroxy-3-oxohexanoate
  • (S)-Tertiary-Butyl-6-Chloro-5-Hydroxy-3-Oxo Hexanoate
  • TERT-BUTYL (S)-6-CHLORO-5-HYDROXY-3-OXOHEXANOATE
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