Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H20S |
| Molecular Weight | 160.32 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCSC
InChI
InChIKey=AHCJTMBRROLNHV-UHFFFAOYSA-N
InChI=1S/C9H20S/c1-3-4-5-6-7-8-9-10-2/h3-9H2,1-2H3
| Molecular Formula | C9H20S |
| Molecular Weight | 160.32 |
| 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 |
|---|---|---|
| The seed composition of Arabidopsis mutants for the group 3 sulfate transporters indicates a role in sulfate translocation within developing seeds. | 2010-10 |
|
| Kinetics and substrate specificities of desulfo-glucosinolate sulfotransferases in Arabidopsis thaliana. | 2009-02 |
|
| Subclade of flavin-monooxygenases involved in aliphatic glucosinolate biosynthesis. | 2008-11 |
|
| Mapping of QTL for resistance against the crucifer specialist herbivore Pieris brassicae in a new Arabidopsis inbred line population, Da(1)-12 x Ei-2. | 2007-06-27 |
|
| [Effectiveness of new quarternary ammonium chloride compounds against selected bacteria and fungi. XXI. Synthesis of alkoxymethyl-3,4-dimethyl- pyridine and 1-ethyloxymethyl-3-alkylthiomethylimidazole chlorides]. | 1989 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:32:21 GMT 2025
by
admin
on
Mon Mar 31 20:32:21 GMT 2025
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| Record UNII |
L68L019D9G
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
METHYL OCTYL SULFIDE
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admin on Mon Mar 31 20:32:21 GMT 2025 , Edited by admin on Mon Mar 31 20:32:21 GMT 2025
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223-029-2
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DTXSID00190470
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L68L019D9G
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