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CAS 1845-25-6

:

(1S,2S,5S)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one

Description:
(1S,2S,5S)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one, with CAS number 1845-25-6, is a bicyclic organic compound characterized by its unique bicyclo[3.1.1]heptane structure, which features a hydroxyl group and a ketone functional group. This compound is typically colorless to pale yellow in appearance and is known for its pleasant, woody, and sweet aroma, making it valuable in the fragrance and flavor industries. The presence of multiple methyl groups contributes to its hydrophobic nature, influencing its solubility in organic solvents rather than in water. Its stereochemistry, indicated by the (1S,2S,5S) configuration, plays a crucial role in its biological activity and interaction with other molecules. Additionally, this compound may exhibit various chemical reactivity patterns typical of ketones and alcohols, such as oxidation and esterification. Overall, its distinctive structure and properties make it an interesting subject for research in organic chemistry and applications in perfumery and flavoring.
Formula:C10H16O2
InChI:InChI=1S/C10H16O2/c1-9(2)6-4-7(9)10(3,12)8(11)5-6/h6-7,12H,4-5H2,1-3H3/t6-,7-,10-/m0/s1
InChI key:InChIKey=VZRRCQOUNSHSGB-BYULHYEWSA-N
SMILES:CC1(C)[C@@]2(C[C@]1(CC(=O)[C@@]2(C)O)[H])[H]
Synonyms:
  • (-)-2-Hydroxy-3-pinanone
  • (-)-2α-Hydroxypinocamphone
  • (1S,2S,5S)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
  • (1S,2S,5S)-2-Hydroxypinan-3-one
  • (2S)-2-hydroxy-2,6,6-trimethyl-norpinan-3-one
  • 2α-Hydroxypinan-3-one
  • 3-Pinanone, 2-hydroxy-, (1S,2S,5S)-(-)-
  • Bicyclo[3.1.1]heptan-3-one, 2-hydroxy-2,6,6-trimethyl-, (1S,2S,5S)-
  • Bicyclo[3.1.1]heptan-3-one, 2-hydroxy-2,6,6-trimethyl-, [1S-(1α,2α,5α)]-
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