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 3-OCTENE, (3E)-

SMILES

CCCC\C=C\CC

InChI

InChIKey=YCTDZYMMFQCTEO-FNORWQNLSA-N
InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h5,7H,3-4,6,8H2,1-2H3/b7-5+

HIDE SMILES / InChI

Molecular Formula C8H16
Molecular Weight 112.2126
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Suzuki cross-coupling approaches to the synthesis of bioactive 3-substituted and 5-substituted-4-methoxy-6-methyl-2-pyrones.
2003 Aug 18
Adducts of phenoxathiin and thianthrene cation radicals with alkenes and cycloalkenes.
2003 Nov 14
Photochemical sources of organic acids. 2. Formation of C5-C9 carboxylic acids from alkene ozonolysis under dry and humid conditions.
2005 Jun 23
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
Multivariate study of different beef quality traits from local Spanish cattle breeds.
2008 Mar
Olefin coordination in copper(I) complexes of bis(2-pyridyl)amine.
2009 Feb 7
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:32:12 GMT 2023
Edited
by admin
on Sat Dec 16 08:32:12 GMT 2023
Record UNII
2A4P9KO860
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-OCTENE, (3E)-
Systematic Name English
TRANS-3-OCTENE
Systematic Name English
.GAMMA.-TRANS-OCTENE
Common Name English
3-OCTENE, (E)-
Systematic Name English
(E)-3-OCTENE
Systematic Name English
NSC-95418
Code English
(3E)-3-OCTENE
Systematic Name English
Code System Code Type Description
PUBCHEM
638228
Created by admin on Sat Dec 16 08:32:12 GMT 2023 , Edited by admin on Sat Dec 16 08:32:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID90872995
Created by admin on Sat Dec 16 08:32:12 GMT 2023 , Edited by admin on Sat Dec 16 08:32:12 GMT 2023
PRIMARY
NSC
95418
Created by admin on Sat Dec 16 08:32:12 GMT 2023 , Edited by admin on Sat Dec 16 08:32:12 GMT 2023
PRIMARY
FDA UNII
2A4P9KO860
Created by admin on Sat Dec 16 08:32:12 GMT 2023 , Edited by admin on Sat Dec 16 08:32:12 GMT 2023
PRIMARY
CAS
14919-01-8
Created by admin on Sat Dec 16 08:32:12 GMT 2023 , Edited by admin on Sat Dec 16 08:32:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
238-990-3
Created by admin on Sat Dec 16 08:32:12 GMT 2023 , Edited by admin on Sat Dec 16 08:32:12 GMT 2023
PRIMARY
CHEBI
88863
Created by admin on Sat Dec 16 08:32:12 GMT 2023 , Edited by admin on Sat Dec 16 08:32:12 GMT 2023
PRIMARY