1686-14-2
Chemical Structure
α-Pinene oxide
- CAS No.: 1686-14-2
- Formula:C10H16O
- Molecular Weight:152.23
IUPAC Name: 2,7,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane
InChIKey: NQFUSWIGRKFAHK-UHFFFAOYSA-N
SMILES: CC12C(CC3CC1O2)C3(C)C
Biological Activity:
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α-Pinene oxide | 96.75% | α-Pinene oxide is a type of monoterpene epoxidation intermediate. α-Pinene oxide is produced via the cytochrome P-450-mediated oxidation pathway in Dendroctonus terebrans body microsomes and rat liver microsomes, and can be further converted into alcohols, ketones and insect pheromone derivatives. α-Pinene oxide can generate the perfume intermediate myrtenal. α-Pinene oxide is used in studies related to terpenoid metabolism and perfume synthesis. |
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α-Pinene oxide (Standard) | ≥98% | α-Pinene oxide (Standard) is the analytical standard of α-Pinene oxide (HY-W130074). This product is intended for research and analytical applications. α-Pinene oxide is a type of monoterpene epoxidation intermediate. α-Pinene oxide is produced via the cytochrome P-450-mediated oxidation pathway in Dendroctonus terebrans body microsomes and rat liver microsomes, and can be further converted into alcohols, ketones and insect pheromone derivatives. α-Pinene oxide can generate the perfume intermediate myrtenal. α-Pinene oxide is used in studies related to terpenoid metabolism and perfume synthesis. | ||||||||||||||||||||
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References
- [1]. White RA Jr, et al. Conversion of α-pinene to α-pinene Oxide by Rat Liver and the Bark Beetle Dendroctonus terebrans Microsomal Fractions. Pesticide Biochemistry and Physiology. 1979;10:233-242.
- [2]. Kaminska J, et al. The isomerization of α-pinene oxide with Brønsted and Lewis acids. Recueil des Travaux Chimiques des Pays-Bas. 1992;111(10):432-437.
- [3]. Liu P, et al. Thermal stability and oxidation characteristics of α-pinene, β-pinene and α-pinene/β-pinene mixture. RSC Adv. 2021 Jun 8;11(33):20529-20540. [Content Brief]
