1,7-OCTADIENE

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 Search

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

Title	Date	PubMed
Ruthenium(II)-catalyzed isomer-selective cyclization of 1,6-dienes leading to exo-methylenecyclopentanes: unprecedented cycloisomerization mechanism involving ruthenacyclopentane(hydrido) intermediate.	2001 Jul 4	11427063
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 Mar 7	11456805
High-throughput evaluation of olefin copolymer composition by means of attenuated total reflection Fourier tranform infrared spectroscopy.	2001 Nov-Dec	11703157
C-H...pi interactions in the low-temperature crystal structures of alpha,omega-unsaturated linear hydrocarbons.	2002 Aug 21	12196939
Hydrosilylation of dienes by yttrium hydrido complexes containing a linked amido-cyclopentadienyl ligand.	2004 Aug 7	15278114
Permeation characteristics of a hydrophilic basic compound across a bio-mimetic artificial membrane.	2004 May 4	15081157
Aromatic and aliphatic hydrocarbon consumption and transformation by the styrene degrading strain Pseudomonas putida CA-3.	2005 Aug 15	16002236
Guerbet reaction of primary alcohols leading to beta-alkylated dimer alcohols catalyzed by iridium complexes.	2006 Oct 13	17025333
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 Aug 3	17602534
Ultrasound assisted phase-transfer catalytic epoxidation of 1,7-octadiene - a kinetic study.	2007 Jan	16571377
Facile, efficient functionalization of polyolefins via controlled incorporation of terminal olefins by repeated 1,7-octadiene insertion.	2007 Nov 21	17958430
Regionally-selective cell colonization of micropatterned surfaces prepared by plasma polymerization of acrylic acid and 1,7-octadiene.	2009	19093722
ESIMS studies and calculations on alkali-metal adduct ions of ruthenium olefin metathesis catalysts and their catalytic activity in metathesis reactions.	2009 Oct 19	19760711
Insight into the phase equilibrium phenomena of systems containing dienes and dicyanamide ionic liquids as a new potential application.	2010 Dec 2	21062074
Rhenium hydride/boron Lewis acid cocatalysis of alkene hydrogenations: activities comparable to those of precious metal systems.	2010 Dec 29	21141863
On the relationship between structure and reaction rate in olefin ring-closing metathesis.	2010 Oct 14	20820538

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 10:03:23 GMT 2023` Edited by `admin` on `Sat Dec 16 10:03:23 GMT 2023`
Record UNII	N4H29T34J2
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

1,7-OCTADIENE

Systematic Name

English

.ALPHA.,.OMEGA.-OCTADIENE

Common Name

English

NSC-82324

Code

English

Code System Code Type Description

NSC

82324