2S3S4Octen2ol

2S3S4Octen2ol is a chemical compound with the molecular formula C8H16O. It is a specific isomer of octenol, which is an alcohol derived from octene. The "2S3S4" designation in the compound's name refers to the stereochemistry of the molecule, indicating that the hydroxyl group (-OH) is attached to the second carbon atom, and the double bond is located between the third and fourth carbon atoms, both in the S (syn) configuration.

2S3S4Octen2ol is a colorless liquid at room temperature and has a characteristic alcohol odor. It is soluble in water and organic solvents. The compound is primarily used as a precursor in the synthesis of various pharmaceuticals and agrochemicals. Its stereospecific nature makes it valuable in the production of enantiomerically pure compounds, which are important in the development of drugs and other biologically active substances.

The synthesis of 2S3S4Octen2ol typically involves the selective reduction of the corresponding octene or the hydration of the corresponding octene oxide. The compound can also be obtained through the asymmetric synthesis, which involves the use of chiral catalysts to produce the desired stereoisomer.

In terms of its chemical properties, 2S3S4Octen2ol is relatively stable under normal conditions but can undergo oxidation to form the corresponding ketone. It can also react with various reagents to form esters, ethers, and other derivatives. The compound's reactivity and selectivity make it a useful intermediate in organic synthesis.