U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H16
Molecular Weight 112.2126
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 2-OCTENE, (2E)-

SMILES

CCCCC\C=C\C

InChI

InChIKey=ILPBINAXDRFYPL-HWKANZROSA-N
InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h3,5H,4,6-8H2,1-2H3/b5-3+

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Olefin coordination in copper(I) complexes of bis(2-pyridyl)amine.
2009-02-07
Rate constants for the gas-phase reactions of OH radicals with a series of C6-C14 alkenes at 299 +/- 2 K.
2009-02-05
Highly regioselective isomerization-hydroformylation of internal olefins to linear aldehyde using rh complexes with tetraphosphorus ligands.
2008-08-21
Multivariate study of different beef quality traits from local Spanish cattle breeds.
2008-03
Highly regioselective hydroformylation with hemispherical chelators.
2008
Identification of components of male-produced pheromone of coffee white stemborer, Xylotrechus quadripes.
2006-01
A comparison of the aroma volatiles and fatty acid compositions of grilled beef muscle from Aberdeen Angus and Holstein-Friesian steers fed diets based on silage or concentrates.
2004-09
Immobilization of oxomolybdenum species in a layered double hydroxide pillared by 2,2'-bipyridine-5,5'-dicarboxylate anions.
2004-08-23
Hydrophosphorylation of alkenes with dialkyl phosphites catalyzed by Mn(III) under air.
2004-08-06
Patents

Patents

Name Type Language
2-OCTENE, (2E)-
Systematic Name English
NSC-97522
Preferred Name English
(E)-2-OCTENE
Systematic Name English
(2E)-2-OCTENE
Systematic Name English
TRANS-2-OCTENE
Systematic Name English
2-OCTENE, (E)-
Systematic Name English
2-OCTENE, TRANS-
Systematic Name English
Code System Code Type Description
CHEBI
88820
Created by admin on Mon Mar 31 22:09:03 GMT 2025 , Edited by admin on Mon Mar 31 22:09:03 GMT 2025
PRIMARY
CAS
13389-42-9
Created by admin on Mon Mar 31 22:09:03 GMT 2025 , Edited by admin on Mon Mar 31 22:09:03 GMT 2025
PRIMARY
PUBCHEM
5364448
Created by admin on Mon Mar 31 22:09:03 GMT 2025 , Edited by admin on Mon Mar 31 22:09:03 GMT 2025
PRIMARY
ECHA (EC/EINECS)
236-463-2
Created by admin on Mon Mar 31 22:09:03 GMT 2025 , Edited by admin on Mon Mar 31 22:09:03 GMT 2025
PRIMARY
FDA UNII
G13G1YR8YW
Created by admin on Mon Mar 31 22:09:03 GMT 2025 , Edited by admin on Mon Mar 31 22:09:03 GMT 2025
PRIMARY
NSC
97522
Created by admin on Mon Mar 31 22:09:03 GMT 2025 , Edited by admin on Mon Mar 31 22:09:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID30872994
Created by admin on Mon Mar 31 22:09:03 GMT 2025 , Edited by admin on Mon Mar 31 22:09:03 GMT 2025
PRIMARY