| Weight | 280.452 g/mol |
|---|---|
| Formula | C18H32O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 13 |
GOSSYPLURE (50933-33-0)
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- Stereochemical control in Wittig olefin synthesis. Preparation of the pink bollworm sex pheromone mixture, gossyplure (Journal of the American Chemical Society, 1975)
- Pink bollworm (Lepidoptera: Gelechiidae): large-scale field trials with a high-rate Gossyplure formulation (Journal of Economic Entomology, 1987)
- Aerial concentrations of gossyplure, the sex pheromone of the pink bollworm (Lepidoptera: Gelechiidae), within and above cotton fields treated with long-lasting dispensers (Environmental Entomology, 1990)
- Trennung und analytische bestimmung synthetischer pheromone am beispiel der isomeren 7,11-hexadecadien-1-ylacetate (gossyplure) (Tetrahedron, 1976)
- Cyclic phosphonium ylides. A short synthesis of gossyplure (Journal of Organic Chemistry, 1981)
- Pink bollworm (Lepidoptera: Gelechiidae): point source density and its relationship to efficacy in attracticide formulations of gossyplure. (Journal of Economic Entomology, 1990)
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SMILESCCCCC=CCCC=CCCCCCCOC(=O)C
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InChIKeyBXJHOKLLMOYSRQ-UHFFFAOYSA-N
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