Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H14 |
| Molecular Weight | 110.1968 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CCCCCC=C
InChI
InChIKey=XWJBRBSPAODJER-UHFFFAOYSA-N
InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-8H2
| Molecular Formula | C8H14 |
| Molecular Weight | 110.1968 |
| 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 |
|---|---|---|
| Rhenium hydride/boron Lewis acid cocatalysis of alkene hydrogenations: activities comparable to those of precious metal systems. | 2010-12-29 |
|
| Insight into the phase equilibrium phenomena of systems containing dienes and dicyanamide ionic liquids as a new potential application. | 2010-12-02 |
|
| On the relationship between structure and reaction rate in olefin ring-closing metathesis. | 2010-10-14 |
|
| ESIMS studies and calculations on alkali-metal adduct ions of ruthenium olefin metathesis catalysts and their catalytic activity in metathesis reactions. | 2009-10-19 |
|
| Regionally-selective cell colonization of micropatterned surfaces prepared by plasma polymerization of acrylic acid and 1,7-octadiene. | 2009 |
|
| Facile, efficient functionalization of polyolefins via controlled incorporation of terminal olefins by repeated 1,7-octadiene insertion. | 2007-11-21 |
|
| Addition of the phenoxathiin cation radical to alkenes and nonconjugated dienes. Formation of (E)- and (Z)-(10-phenoxathiiniumyl)alkenes and (E)- and (Z)-(10-phenoxathiiniumyl)dienes on basic alumina. | 2007-08-03 |
|
| Ultrasound assisted phase-transfer catalytic epoxidation of 1,7-octadiene - a kinetic study. | 2007-01 |
|
| Guerbet reaction of primary alcohols leading to beta-alkylated dimer alcohols catalyzed by iridium complexes. | 2006-10-13 |
|
| Aromatic and aliphatic hydrocarbon consumption and transformation by the styrene degrading strain Pseudomonas putida CA-3. | 2005-08-15 |
|
| Hydrosilylation of dienes by yttrium hydrido complexes containing a linked amido-cyclopentadienyl ligand. | 2004-08-07 |
|
| Permeation characteristics of a hydrophilic basic compound across a bio-mimetic artificial membrane. | 2004-05-04 |
|
| C-H...pi interactions in the low-temperature crystal structures of alpha,omega-unsaturated linear hydrocarbons. | 2002-08-21 |
|
| High-throughput evaluation of olefin copolymer composition by means of attenuated total reflection Fourier tranform infrared spectroscopy. | 2001-11-13 |
|
| Ruthenium(II)-catalyzed isomer-selective cyclization of 1,6-dienes leading to exo-methylenecyclopentanes: unprecedented cycloisomerization mechanism involving ruthenacyclopentane(hydrido) intermediate. | 2001-07-04 |
|
| Remarkable control of radical cyclization processes of cyclic enyne: total syntheses of (+/-)-methyl gummiferolate, (+/-)-methyl 7beta-hydroxykaurenoate, and (+/-)-methyl 7-oxokaurenoate and formal synthesis of (+/-)-gibberellin a(12) from a common synthetic precursor. | 2001-03-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:59:47 GMT 2025
by
admin
on
Mon Mar 31 22:59:47 GMT 2025
|
| Record UNII |
N4H29T34J2
|
| Record Status |
Validated (UNII)
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| Record Version |
|
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Systematic Name | English | ||
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Preferred Name | English | ||
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Common Name | English |
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82324
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3710-30-3
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223-054-9
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19460
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N4H29T34J2
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DTXSID6063147
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1,7-Octadiene
Created by
admin on Mon Mar 31 22:59:47 GMT 2025 , Edited by admin on Mon Mar 31 22:59:47 GMT 2025
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