2,4,5-Trimethoxypropiophenone
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Names | |
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IUPAC name
1-(3,4,5-Trimethoxyphenyl)propan-1-one | |
Other names
Isoacoramone 2,4,5-Trimethoxypropiophenone | |
Identifiers | |
4-08-00-02746 | |
3904-18-5 | |
ChemSpider | 610798 |
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Jmol-3D images | Image |
PubChem | 700861 |
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Properties | |
Molecular formula |
C12H16O4 |
Molar mass | 224.25 g·mol−1 |
Melting point | 109 °C (228 °F; 382 K) |
Boiling point | 186 °C (367 °F; 459 K) |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
2,4,5-Trimethoxypropiophenone is a natural phenylpropanoid and precursor in the synthesis of α-asarone.[1]
Natural Occurrence
2,4,5-Trimethoxypropiophenone is a component of several plant species' essential oils. The chemical has been identified in Piper marginatum,[2] Acorus tatarinowii,[3] and Asarum maximum.[4]
References
- ↑ Francisco, Díaz; Leticia, Contreras; Rosa, Flores; Joaquín, Tamariz; Fernando, Labarrios; Germán, Chamorro; Héber, Muñoz (1991). "An Efficient Synthesis of α-Asarone". Organic Preparations and Procedures International 23 (2): 133–138. doi:10.1080/00304949109458299.
- ↑ Oliveira Santos, Bárbara Viviana; Oliveira Chaves, Maria Célia (1999). "2,4,5-Trimethoxypropiophenone from Piper marginatum". Biochemical Systematics and Ecology 27 (5): 539–541. doi:10.1016/S0305-1978(98)00109-4.
- ↑ Jinfeng, Hu; Xiaozhang, Feng (2000). "Phenylpropanes from Acorus tatarinowii". Planta Medica 66 (7): 662–664. doi:10.1055/s-2000-8628.
- ↑ X., Wang; Long, C.; Cai, S.; Zhao, Y. (2000). Zhong cao yao 31 (12): 888–890.