2649-68-5

Usage

Uses

Used in Chemical Industry:
Clovanediol diacetate is used as a solvent for its ability to dissolve a wide range of substances, enhancing the manufacturing process of various chemical products.
Used in Plastics and Polymer Industry:
Clovanediol diacetate is used as a plasticizer to increase the flexibility and workability of polymers, improving their performance in end-use applications.
Used in Manufacturing of Resins:
Clovanediol diacetate is used as a key component in the production of resins, contributing to their stability and durability.
Used in Coatings Industry:
Clovanediol diacetate is used in the formulation of coatings to provide a low evaporation rate, enhancing the longevity and resistance to environmental factors such as ultraviolet light.
Used in Thermoplastic Materials:
Clovanediol diacetate is used in the production of thermoplastic materials, where its properties contribute to the material's flexibility and resistance to degradation.
While Clovanediol diacetate is generally regarded as safe for industrial use, it is important to note that over-exposure can lead to eye and skin irritation, breathing difficulties, and potential harm to aquatic life. Proper handling and safety measures should be implemented to minimize these risks.

Upstream product

• 2649-64-1 clovanediol 
• 108-24-7 acetic anhydride 

Relevant academic research and scientific papers

Constituents of Sindora sumatrana MIQ. I. Isolation and NMR spectral analysis of sesquiterpenes from the dried pods

Investigation of the neutral fraction of the dried pods of Sindora sumatrana MIQ. has resulted in the isolation of three new sesquiterpenoids (2, 6 and 8) together with nine known ones (1, 3, 4, 5, 7, 9, 10, 11a and 12a), of which three (7, 10 and 12a) are reported for the first time from a natural source. One other compound, 4-stigmasten-3-one (13) (together with a sterol mixture; β-sitosterol, stigmasterol and campesterol) was also obtained. The structures of all the isolated sesquiterpenes were determined by means of spectroscopic methods, mainly two-dimensional NMR techniques, and the compounds were found to have the caryophyllane, humulane, clovane and caryolane skeletons. The NMR data of the isolated sesquiterpenes are also discussed.

Constituents of Sindora sumatrana MIQ. II. Five new sesquiterpenoids from the dried pods

Further investigation of the neutral fraction of the methanolic extract of Sindora sumatrana MIQ. (Leguminosae) has yielded five new sesquiterpenoids: a new trans-isodaucane diol (1), two caryophyllane-type epoxydiols (2, 3), the diacetate of a caryophyllane-type trialcohol (4) and a caryolane-type hydroxy-ketone (5) which possesses an α-C-12 methano bridge. The structure elucidation of the compounds was based mainly on two-dimensional NMR techniques. The biosynthetic significance of the acid-catalyzed rearrangement of 5 to give a clovane-type hydroxyketone (10) is also discussed.