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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H12O
Molecular Weight 124.1803
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of 2,4-OCTADIENAL, (2E,4E)-

SMILES

CCC\C=C\C=C\C=O

InChI

InChIKey=DVVATNQISMINCX-YTXTXJHMSA-N
InChI=1S/C8H12O/c1-2-3-4-5-6-7-8-9/h4-8H,2-3H2,1H3/b5-4+,7-6+

HIDE SMILES / InChI

Molecular Formula C8H12O
Molecular Weight 124.1803
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 2
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Conventional and unconventional antimicrobials from fish, marine invertebrates and micro-algae.
2010-04-14
Teratogenic effects of diatom metabolites on sea urchin Paracentrotus lividus embryos.
2010-03-30
The influence of bioactive oxylipins from marine diatoms on invertebrate reproduction and development.
2009-08-21
High plasticity in the production of diatom-derived polyunsaturated aldehydes under nutrient limitation: physiological and ecological implications.
2009-08
Fragrant unsaturated aldehydes elicit activation of the Keap1/Nrf2 system leading to the upregulation of thioredoxin expression and protection against oxidative stress.
2009-05
Identification of the airborne aggregation pheromone of the common bed bug, Cimex lectularius.
2008-06
Differential effect of three polyunsaturated aldehydes on marine bacterial isolates.
2008-01-31
Growth inhibition of cultured marine phytoplankton by toxic algal-derived polyunsaturated aldehydes.
2007-12-15
Semiochemical investigations of the insidious flower bug, Orius insidiosus (Say).
2007-08
Biosynthetic intermediates and stereochemical aspects of aldehyde biosynthesis in the marine diatom Thalassiosira rotula.
2006-02
Cytotoxicity of diatom-derived oxylipins in organisms belonging to different phyla.
2004-08
Production of octadienal in the marine diatom Skeletonema costatum.
2003-03-20
Effect of oleic and linoleic acids on the production of deep-fried odor in heated triolein and trilinolein.
2001-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:29:53 GMT 2025
Edited
by admin
on Mon Mar 31 19:29:53 GMT 2025
Record UNII
PR4J26TQJD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 3721
Preferred Name English
2,4-OCTADIENAL, (2E,4E)-
Systematic Name English
2,4-OCTADIEN-1-AL, (E,E)-
Systematic Name English
2,4-OCTADIENAL, TRANS,TRANS-
Systematic Name English
TRANS,TRANS-2,4-OCTADIENAL [FHFI]
Common Name English
(E,E)-2,4-OCTADIEN-1-AL
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
250-147-1
Created by admin on Mon Mar 31 19:29:53 GMT 2025 , Edited by admin on Mon Mar 31 19:29:53 GMT 2025
PRIMARY
CAS
5577-44-6
Created by admin on Mon Mar 31 19:29:53 GMT 2025 , Edited by admin on Mon Mar 31 19:29:53 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
EPA CompTox
DTXSID00885475
Created by admin on Mon Mar 31 19:29:53 GMT 2025 , Edited by admin on Mon Mar 31 19:29:53 GMT 2025
PRIMARY
CAS
30361-28-5
Created by admin on Mon Mar 31 19:29:53 GMT 2025 , Edited by admin on Mon Mar 31 19:29:53 GMT 2025
PRIMARY
FDA UNII
PR4J26TQJD
Created by admin on Mon Mar 31 19:29:53 GMT 2025 , Edited by admin on Mon Mar 31 19:29:53 GMT 2025
PRIMARY
PUBCHEM
5283329
Created by admin on Mon Mar 31 19:29:53 GMT 2025 , Edited by admin on Mon Mar 31 19:29:53 GMT 2025
PRIMARY
JECFA MONOGRAPH
1172
Created by admin on Mon Mar 31 19:29:53 GMT 2025 , Edited by admin on Mon Mar 31 19:29:53 GMT 2025
PRIMARY