CAS 24047-72-1
:(1R,2R,5R)-(+)-2-hydroxy-3-pinanone
Description:
(1R,2R,5R)-(+)-2-hydroxy-3-pinanone, with the CAS number 24047-72-1, is a chiral organic compound belonging to the class of ketones. It features a bicyclic structure derived from pinane, characterized by a hydroxyl group (-OH) and a carbonyl group (C=O) within its molecular framework. This compound is typically colorless to pale yellow and has a pleasant, pine-like aroma, making it of interest in the fragrance and flavor industries. Its stereochemistry, indicated by the (1R,2R,5R) configuration, contributes to its unique properties and potential applications in synthesizing other chiral molecules. The presence of the hydroxyl group also suggests that it can participate in hydrogen bonding, influencing its solubility and reactivity. Additionally, (1R,2R,5R)-(+)-2-hydroxy-3-pinanone may exhibit biological activity, which warrants further investigation for potential uses in pharmaceuticals or agrochemicals. Overall, its distinct structural features and properties make it a valuable compound in various chemical applications.
Formula:C10H16O2
InChI:InChI=1/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-/m1/s1
SMILES:CC1(C)[C@@H]2C[C@H]1[C@](C)(C(=O)C2)O
Synonyms:- (1R,2R,5R)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
- bicyclo[3.1.1]heptan-3-one, 2-hydroxy-2,6,6-trimethyl-, (1R,2R,5R)-
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Found 6 products.
(1R,2R,5R)-(+)-2-Hydroxy-3-pinanone
CAS:Formula:C10H16O2Purity:>98.0%(GC)Color and Shape:White or Colorless to Light yellow powder to lump to clear liquidMolecular weight:168.24(1R,2R,5R)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
CAS:Formula:C10H16O2Purity:97%Color and Shape:SolidMolecular weight:168.2328(1R,2R,5R)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
CAS:<p>(1R,2R,5R)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one</p>Purity:97%Molecular weight:168.24g/mol(+)-(1R,2R,5R)-2-Hydroxy-3-pinanone
CAS:<p>(+)-(1R,2R,5R)-2-Hydroxy-3-pinanone is an organic compound that can be prepared by a kinetic resolution of the racemic mixture of (+)-(1S,2S,5S)-2-hydroxy-3-pinanone. This reaction is performed in two steps: first the racemic mixture is converted to the corresponding chiral acetylacetonate by reaction with acetic anhydride followed by hydrolysis with sodium hydroxide. The pentane reacts with the ring opening of the acetylacetonate to give (+)-(1R,2R,5R)-2-hydroxypinanone and its enantiomer. The nature of this preparative method means that it is not possible to recover (+)-(1R,2R,5R)-2-hydroxypinanone from the reaction products.</p>Formula:C10H16O2Purity:Min. 95%Color and Shape:PowderMolecular weight:168.23 g/mol(1R,2R,5R)-(+)-2-Hydroxy-3-pinanone
CAS:Formula:C10H16O2Purity:97%Color and Shape:SolidMolecular weight:168.236(+)-(1R,2R,5R)-2-Hydroxy-3-pinanone
CAS:Controlled ProductFormula:C10H16O2Color and Shape:NeatMolecular weight:168.23






