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Atomfair [(1R,2S)-2-hydroxycyclohexyl] acetate C8H14O3

Description [(1R,2S)-2-hydroxycyclohexyl] acetate (CAS No. 13858-62-3) is a high-purity chiral compound with the molecular formula C8H14O3. This stereospecific acetate derivative of cyclohexanediol is widely utilized in organic synthesis, pharmaceutical research, and fragrance applications due to its unique structural and stereochemical properties. The compound is supplied as a clear, colorless to pale-yellow liquid with a characteristic mild ester-like odor. It is rigorously tested for purity (typically ??97% by GC) and stored under controlled conditions to ensure stability. [(1R,2S)-2-hydroxycyclohexyl] acetate is particularly valuable for asymmetric synthesis, chiral auxiliaries, and as a building block for complex molecules. Proper handling requires storage in a…

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Description

Description

[(1R,2S)-2-hydroxycyclohexyl] acetate (CAS No. 13858-62-3) is a high-purity chiral compound with the molecular formula C8H14O3. This stereospecific acetate derivative of cyclohexanediol is widely utilized in organic synthesis, pharmaceutical research, and fragrance applications due to its unique structural and stereochemical properties. The compound is supplied as a clear, colorless to pale-yellow liquid with a characteristic mild ester-like odor. It is rigorously tested for purity (typically ??97% by GC) and stored under controlled conditions to ensure stability. [(1R,2S)-2-hydroxycyclohexyl] acetate is particularly valuable for asymmetric synthesis, chiral auxiliaries, and as a building block for complex molecules. Proper handling requires storage in a cool, dry place under inert atmosphere to prevent hydrolysis or racemization.

  • CAS No: 13858-62-3
  • Molecular Formula: C8H14O3
  • Molecular Weight: 158.19
  • Exact Mass: 158.094294304
  • Monoisotopic Mass: 158.094294304
  • IUPAC Name: [(1R,2S)-2-hydroxycyclohexyl] acetate
  • SMILES: CC(=O)O[C@@H]1CCCC[C@@H]1O
  • Synonyms: 13858-62-3, 1,2-Cyclohexanediol, 1-acetate, (1R,2S)-rel-

Application

This chiral acetate serves as a key intermediate in the synthesis of enantiomerically pure pharmaceuticals and agrochemicals. Researchers employ it as a stereospecific building block for prostaglandin analogs and other bioactive molecules. The compound’s hydroxyl and acetate functional groups allow for diverse chemical modifications, making it valuable for structure-activity relationship studies. In fragrance chemistry, it contributes to woody-herbal scent profiles in specialty perfumery.

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