2R3R4Octen2ol

2R3R4Octen2ol is an organic compound with the molecular formula C8H16O. It is a specific isomer of octen-2-ol, characterized by the presence of a hydroxyl group (-OH) at the second carbon atom and a double bond between the third and fourth carbon atoms. The "2R3R4" designation indicates the stereochemistry of the molecule, with the R configuration at the second and fourth carbon atoms and the S configuration at the third carbon atom.

2R3R4Octen2ol is a secondary alcohol, meaning the hydroxyl group is attached to a saturated carbon atom. This compound is a colorless liquid at room temperature and has a characteristic alcohol odor. It is soluble in water and organic solvents.

The synthesis of 2R3R4Octen2ol typically involves the reduction of an appropriate alkene or the hydration of an alkyne, followed by stereoselective reduction to achieve the desired stereochemistry. The compound is used in various chemical syntheses, particularly in the preparation of more complex organic molecules.

2R3R4Octen2ol is also a useful intermediate in the production of pharmaceuticals and other fine chemicals. Its stereospecific nature makes it valuable in asymmetric synthesis, where the control of stereochemistry is crucial for the production of enantiomerically pure compounds.

In summary, 2R3R4Octen2ol is a specific isomer of octen-2-ol with a unique stereochemistry and a range of applications in organic synthesis and pharmaceutical production. Its properties and synthesis methods make it an important compound in the field of organic chemistry.