Chemical Properties of Terpinen-4-ol (CAS 562-74-3).
Objective: A study was conducted to find new highly active insecticidal compounds in terpinen-4-ol. Method: Six new derivatives were synthesized using terpinen-4-ol as staring materials and their structures had been confirmed by NMR, IR and MS. The insecticidal activity of the eight derivatives on Musca domestica had been determined. Result: The derivatives almost exhibited stronger fumigant.
Terpinen-4-ol is a kind of natural terpene alcohol isolated from essential oil, it is widely used in flavors and fragrances and in reconstitution of essential oil such as rose, lavender and geranium. On the other hand, terpinen-4-ol has strong effects of disinfection, sterilization and antisepsis, it can also be used as natural disinfectant to treat illness and hurts.
Recent advancements in the area of organic polymer applications demand novel and advanced materials with desirable surface, optical and electrical properties to employ in emerging technologies. This study examines the fabrication and characterization of polymer thin films from non-synthetic Terpinen-4-ol monomer using radio frequency plasma polymerization.
The synthesis process involved the introduction of terpinen-4-ol monomer units (a monocyclic terpene alcohol extracted from the distillation of Melaleuca alternifolia oil) into a radio frequency glow discharge.
Azaindoles are rare in nature but extremely attractive for drug discovery programs. Azaindoles can be obtained by diverse methods, including those involving metal-catalyzed reactions. This important core has been fascinating the scientific community due to their challenging synthesis and relevant bioactivity. This paper highlights the diverse synthetic methodologies developed to date involving.
Terpinen-4-ol, a naturally occurring monoterpene, is the main bioactive component of tea-tree oil and has been shown to have many biological activities such as antifungal properties.
Description Terpineol is a monoterpenealcoholthat has been isolated from a variety of sources such as cajuput oil, pine oil, and petitgrainoil. There are four isomers, alpha-, beta-, gamma-terpineol, and terpinen-4-ol. Beta- and gamma-terpineol differ only by the location of the double bond.