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4-Vinylanisole

From Wikipedia, the free encyclopedia
4-Vinylanisole
Names
Preferred IUPAC name
1-Ethenyl-4-methoxybenzene
Other names
p-vinylanisole, 4-methoxystyrene
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.010.272Edit this at Wikidata
EC Number
  • 211-298-9
UNII
  • InChI=1S/C9H10O/c1-3-8-4-6-9(10-2)7-5-8/h3-7H,1H2,2H3
    Key: UAJRSHJHFRVGMG-UHFFFAOYSA-N
  • COC1=CC=C(C=C1)C=C
Properties
C9H10O
Molar mass134.178 g·mol−1
Appearancecolorless liquid
Density1.001 g/cm3
Melting point2 °C (36 °F; 275 K)
Boiling point205 °C (401 °F; 478 K)
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315,H319
P264,P280,P302+P352,P305+P351+P338,P321,P332+P313,P337+P313,P362
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

4-Vinylanisole is anorganic 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 modifiedpolystyrenes.[2] It is an aggregationpheromone used by locusts.[3]

References

[edit]
  1. ^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.Bibcode:2012JAFC...6010433Z.doi:10.1021/jf302615s.PMID 23020223.
  2. ^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.Bibcode:1998JAChS.120..888M.doi:10.1021/JA964144I.
  3. ^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.Bibcode:2020Natur.584..584G.doi:10.1038/s41586-020-2610-4.PMID 32788724.S2CID 221106319.
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