Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H16O2 |
| Molecular Weight | 156.2221 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CCC2(CCCCO2)OC1
InChI
InChIKey=GBBVHDGKDQAEOT-UHFFFAOYSA-N
InChI=1S/C9H16O2/c1-3-7-10-9(5-1)6-2-4-8-11-9/h1-8H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Efficacy of new mass-trapping devices against Bactrocera oleae (Diptera tephritidae) for minimizing pesticide input in agroecosystems. | 2009-06 |
|
| Energetics of oxaspirocycle prototypes: 1,7-dioxaspiro[5.5]undecane and 1,7,9-trioxadispiro[5.1.5.3]hexadecane. | 2006-11-24 |
|
| Spiroacetal biosynthesis: (+/-)-1,7-dioxaspiro[5.5]undecane in Bactrocera cacuminata and Bactrocera oleae (Olive Fruit Fly). | 2005-03-17 |
|
| Synthesis of haptens and development of an immunoassay for the olive fruit fly pheromone. | 2004-07-14 |
|
| [(18)O]-oxygen incorporation reveals novel pathways in spiroacetal biosynthesis by Bactrocera cacuminata and B. cucumis. | 2002-07-03 |
|
| Sex pheromone biosynthesis in the female olive fruit-fly. Double labelling from [18O2]-dioxygen into 1,7-dioxaspiro[5.5]undecane. | 2002-06-21 |
|
| Combinatorial synthesis of natural product-like molecules using a first-generation spiroketal scaffold. | 2002-02-08 |
|
| Non-covalent interactions in the crystallization of the enantiomers of 1,7-dioxaspiro. | 2001-06 |
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EPA PESTICIDE CODE |
124851
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67437
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180-84-7
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205-870-7
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KHI3QEQ4ZJ
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DTXSID2040735
Created by
admin on Mon Mar 31 19:20:55 GMT 2025 , Edited by admin on Mon Mar 31 19:20:55 GMT 2025
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PRIMARY |
SUBSTANCE RECORD