Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H30O |
| Molecular Weight | 262.4302 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCC1=CC=C(O)C=C1
InChI
InChIKey=KJWMCPYEODZESQ-UHFFFAOYSA-N
InChI=1S/C18H30O/c1-2-3-4-5-6-7-8-9-10-11-12-17-13-15-18(19)16-14-17/h13-16,19H,2-12H2,1H3
| Molecular Formula | C18H30O |
| Molecular Weight | 262.4302 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006-11 |
|
| Photoregulated transmembrane charge separation by linked spiropyran-anthraquinone molecules. | 2006-01-25 |
|
| The endocrine disruptors nonylphenol and octylphenol exert direct effects on T cells to suppress Th1 development and enhance Th2 development. | 2004-06-15 |
|
| Immature rat uterotrophic assay of 18 chemicals and Hershberger assay of 30 chemicals. | 2003-02-01 |
|
| The branched-chain dodecylbenzene sulfonate degradation pathway of Pseudomonas aeruginosa W51D involves a novel route for degradation of the surfactant lateral alkyl chain. | 1999-08 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:49:12 GMT 2025
by
admin
on
Mon Mar 31 20:49:12 GMT 2025
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| Record UNII |
EZF5Y6P2G8
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID1022508
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66030
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203-202-9
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300000053022
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