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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 4-OCTENE, (4E)-

SMILES

CCC\C=C\CCC

InChI

InChIKey=IRUCBBFNLDIMIK-BQYQJAHWSA-N
InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h7-8H,3-6H2,1-2H3/b8-7+

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
Z-selective olefin metathesis processes catalyzed by a molybdenum hexaisopropylterphenoxide monopyrrolide complex.
2009-06-17
Pulsed-addition ring-opening metathesis polymerization: catalyst-economical syntheses of homopolymers and block copolymers.
2009-03-11
Photochemistry of sulfilimine-based nitrene precursors: generation of both singlet and triplet benzoylnitrene.
2007-08-31
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
Kinetic and spectroscopic studies of the [palladium(Ar-bian)]-catalyzed semi-hydrogenation of 4-octyne.
2005-11-09
Transition-metal-promoted hydroboration of alkenes: a unique reversal of regioselectivity.
2002-04-19
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:14:21 GMT 2025
Edited
by admin
on Mon Mar 31 19:14:21 GMT 2025
Record UNII
FKZ5737B1W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-73940
Preferred Name English
4-OCTENE, (4E)-
Systematic Name English
.DELTA.-TRANS-OCTENE
Common Name English
4-OCTENE, (E)-
Systematic Name English
(E)-4-OCTENE
Systematic Name English
4-OCTENE, TRANS-
Systematic Name English
TRANS-4-OCTENE
Systematic Name English
Code System Code Type Description
FDA UNII
FKZ5737B1W
Created by admin on Mon Mar 31 19:14:21 GMT 2025 , Edited by admin on Mon Mar 31 19:14:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
238-913-3
Created by admin on Mon Mar 31 19:14:21 GMT 2025 , Edited by admin on Mon Mar 31 19:14:21 GMT 2025
PRIMARY
CAS
14850-23-8
Created by admin on Mon Mar 31 19:14:21 GMT 2025 , Edited by admin on Mon Mar 31 19:14:21 GMT 2025
PRIMARY
PUBCHEM
5357253
Created by admin on Mon Mar 31 19:14:21 GMT 2025 , Edited by admin on Mon Mar 31 19:14:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID10872997
Created by admin on Mon Mar 31 19:14:21 GMT 2025 , Edited by admin on Mon Mar 31 19:14:21 GMT 2025
PRIMARY
NSC
73940
Created by admin on Mon Mar 31 19:14:21 GMT 2025 , Edited by admin on Mon Mar 31 19:14:21 GMT 2025
PRIMARY