Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H34 |
| Molecular Weight | 238.4519 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCCCC=C
InChI
InChIKey=ADOBXTDBFNCOBN-UHFFFAOYSA-N
InChI=1S/C17H34/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3H,1,4-17H2,2H3
| Molecular Formula | C17H34 |
| Molecular Weight | 238.4519 |
| 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 |
|---|---|---|
| Chemical profiles, division of labor and social status in Pachycondyla queens (Hymenoptera: formicidae). | 2001 Apr |
|
| Determination of semivolatile compounds in Baltic herring (Clupea harengus membras) by supercritical fluid extraction-supercritical fluid chromatography-gas chromatography-mass spectrometry. | 2002 Mar 27 |
|
| Variability of hydrocarbon and fatty acid components in cultures of the filamentous cyanobacterium Scytonema sp. isolated from microbial community "black cover" of limestone walls in Jerusalem. | 2002 Nov |
|
| Rate constants for reactions of alkyl radicals with water and methanol complexes of triethylborane. | 2007 Jul 6 |
|
| Chrysomelidial in the opisthonotal glands of the oribatid mite, Oribotritia berlesei. | 2008 Aug |
|
| Identification of an Alkylhydroquinone from Rhus succedanea as an Inhibitor of Tyrosinase and Melanogenesis. | 2009 Mar 25 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:51:41 GMT 2023
by
admin
on
Fri Dec 15 19:51:41 GMT 2023
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| Record UNII |
P33057D09T
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| Record Status |
Validated (UNII)
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| Record Version |
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