Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C8H14O |
| Molecular Weight | 126.1962 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCC(O)C#C
InChI
InChIKey=VUGRNZHKYVHZSN-UHFFFAOYSA-N
InChI=1S/C8H14O/c1-3-5-6-7-8(9)4-2/h2,8-9H,3,5-7H2,1H3
| Molecular Formula | C8H14O |
| Molecular Weight | 126.1962 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Characterization of an enantioselective odorant receptor in the yellow fever mosquito Aedes aegypti. | 2009-09-15 |
|
| Reverse and conventional chemical ecology approaches for the development of oviposition attractants for Culex mosquitoes. | 2008-08-22 |
|
| Evaluation of the enantiomers of 1-octen-3-ol and 1-octyn-3-ol as attractants for mosquitoes associated with a freshwater swamp in Florida, U.S.A. | 2007-12 |
|
| A straightforward synthesis of (-)-phaseolinic acid. | 2004-11-12 |
|
| Novel chemoenzymatic strategy for the synthesis of enantiomerically pure secondary alcohols with sterically similar substituents. | 2003-06-27 |
|
| Practical enantioresolution of alcohols with 2-methoxy-2-(1-naphthyl)propionic acid and determination of their absolute configurations by the (1)H NMR anisotropy method. | 2002-01 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:50:25 GMT 2025
by
admin
on
Mon Mar 31 21:50:25 GMT 2025
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| Record UNII |
DG52FEN1K1
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| Record Status |
Validated (UNII)
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| Record Version |
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212-455-4
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DTXSID7022124
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DG52FEN1K1
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13166
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818-72-4
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |