Chemistry:4-Vinylanisole
From HandWiki
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| Names | |
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| Preferred IUPAC name
1-Ethenyl-4-methoxybenzene | |
| Other names
p-vinylanisole, 4-methoxystyrene
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C9H10O | |
| Molar mass | 134.178 g·mol−1 |
| Appearance | colorless liquid |
| Density | 1.001 g/cm3 |
| Melting point | 2 °C (36 °F; 275 K) |
| Boiling point | 205 °C (401 °F; 478 K) |
| Hazards | |
| GHS pictograms | 
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| GHS Signal word | Warning |
| H315, H319 | |
| P264, P280, P302+352, P305+351+338, P321, P332+313, P337+313, P362 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
4-Vinylanisole is an organic compound with the formula CH3OC6H4CH=CH2. It is one of three isomers of vinylanisole. A colorless liquid, 4-vinylanisole is found in a number of foods and drinks.[1] It is also a monomer for the synthesis of modified polystyrenes.[2] It is an aggregation pheromone used by locusts.[3]
References
- ↑ Zhang, Suying; Mueller, Christoph (2012). "Comparative Analysis of Volatiles in Traditionally Cured Bourbon and Ugandan Vanilla Bean (Vanilla planifolia) Extracts". Journal of Agricultural and Food Chemistry 60 (42): 10433–10444. doi:10.1021/jf302615s. PMID 23020223.
- ↑ Mecking, Stefan; Johnson, Lynda K.; Wang, Lin; Brookhart, Maurice (1998). "Mechanistic Studies of the Palladium-Catalyzed Copolymerization of Ethylene and α-Olefins with Methyl Acrylate". Journal of the American Chemical Society 120 (5): 888–899. doi:10.1021/JA964144I. http://nbn-resolving.de/urn:nbn:de:bsz:352-opus-61868.
- ↑ Guo, Xiaojiao; Yu, Qiaoqiao; Chen, Dafeng; Wei, Jianing; Yang, Pengcheng; Yu, Jia; Wang, Xianhui; Kang, Le (2020). "4-Vinylanisole is an aggregation pheromone in locusts". Nature 584 (7822): 584–588. doi:10.1038/s41586-020-2610-4. PMID 32788724. Bibcode: 2020Natur.584..584G.
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