20347-65-3
Chemical Structure
(+)-Bornyl acetate
- CAS No.: 20347-65-3
- Formula:C12H20O2
- Molecular Weight:196.29
IUPAC Name: (1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl acetate
InChIKey: KGEKLUUHTZCSIP-SCVCMEIPSA-N
SMILES: CC1(C)[C@]2(C)[C@@H](OC(C)=O)C[C@@]1([H])CC2
Biological Activity: (+)-Bornyl acetate is a volatile organic compound and a characteristic component of coniferous tree essential oils, including pine needle essential oil. (+)-Bornyl acetate exerts a strong inhibitory effect on root growth of Arabidopsis thaliana seedlings. (+)-Bornyl acetate can induce adult male Periplaneta americana to exhibit sexual behavior and possesses sex pheromone-like activity[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(+)-Bornyl acetate | 98.0% | (+)-Bornyl acetate is a volatile organic compound and a characteristic component of coniferous tree essential oils, including pine needle essential oil. (+)-Bornyl acetate exerts a strong inhibitory effect on root growth of Arabidopsis thaliana seedlings. (+)-Bornyl acetate can induce adult male Periplaneta americana to exhibit sexual behavior and possesses sex pheromone-like activity. | ||||||||||||||||||||
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- [1]. Horiuchi J‑I, et al. Exposing Arabidopsis seedlings to borneol and bornyl acetate affects root growth: Specificity due to the chemical and optical structures of the compounds. Journal of Plant Interactions. 2007;2:101‑104.
- [2]. Allen MS, et al. Chemical and microbiological remote functionalisation of (+)- and (−)-bornyl acetate. Can J Chem. 1979;57(7):733–741.
- [3]. Manabe S, et al. Sex pheromonal activity of (+)-bornyl acetate and related compounds to the American cockroach. Journal of chemical ecology. 1983 Mar;9(3):433-48.
- [4]. Chruszcz‑Lipska K, et al. In situ analysis of chiral components of pictae essential oil by means of ROA spectroscopy: experimental and theoretical Raman and ROA spectra of bornyl acetate. Journal of Raman Spectroscopy. 2011;42(11):1970‑1979.
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