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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
Structure of 1,7-OCTADIENE

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:59:47 GMT 2025
Edited
by admin
on Mon Mar 31 22:59:47 GMT 2025
Record UNII
N4H29T34J2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,7-OCTADIENE
Systematic Name English
NSC-82324
Preferred Name English
.ALPHA.,.OMEGA.-OCTADIENE
Common Name English
Code System Code Type Description
NSC
82324
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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CAS
3710-30-3
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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ECHA (EC/EINECS)
223-054-9
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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PUBCHEM
19460
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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FDA UNII
N4H29T34J2
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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EPA CompTox
DTXSID6063147
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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WIKIPEDIA
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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