3D-FH24244 - 1s2s5s-2-hydroxy-3-pinanone
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(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(1S,2S,5S)-(-)-2-Hydroxy-3-pinanone
CAS:Formula:C10H16O2Purity:>98.0%(GC)Color and Shape:White to Almost white powder to lumpMolecular weight:168.24(1S,2S,5S)-(-)-2-Hydroxy-3-Pinanone
CAS:(1S,2S,5S)-(-)-2-Hydroxy-3-PinanonePurity:98%Molecular weight:168.24g/mol(+)-(1R,2R,5R)-2-Hydroxy-3-pinanone
CAS:(+)-(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.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(+)-Pinanone
CAS:(+)-Pinanone is a bicyclic monoterpene ketone, which is derived from natural sources such as the oxidation of pinene, a compound frequently found in pine trees. As a chiral molecule, (+)-Pinanone exhibits enantiomeric properties, making it significant in stereochemical applications. Its mode of action involves interaction with olfactory receptors, contributing to its role in fragrance synthesis.Formula:C10H16OPurity:Min. 95%Molecular weight:152.23 g/mol(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(1S,2S,5S)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
CAS:Formula:C10H16O2Purity:98%Color and Shape:SolidMolecular weight:168.2328(+)-2-Hydroxypinocamphone
CAS:Controlled ProductApplications (+)-2-Hydroxypinocamphone is an essential oil of inflorescence and leaf of various species of Thymus L. These essential oils were shown to be useful for medical, flavoring and food preservation purposes.
References Hoeferi, M., et al.: Ernahrung., 37, 197 (2013);Formula:C10H16O2Color and Shape:NeatMolecular weight:168.23(+)-(1R,2R,5R)--Ethyl [(2-Hydroxypinan-3-ylene)amino]acetate
CAS:Controlled ProductApplications (+)-(1R,2R,5R)-2-Hydroxy-3-pinanone (H952000) derivative. Intermediate in the synthesis of D-erythro-Sphingosine (S681000).
Formula:C14H23NO3Color and Shape:NeatMolecular weight:253.34(1R,2R,5R)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
CAS:(1R,2R,5R)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-onePurity:97%Molecular weight:168.24g/mol(1S,2S,5S)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
CAS:Formula:C10H16O2Purity:98%Color and Shape:SolidMolecular weight:168.236
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