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Details

Stereochemistry ACHIRAL
Molecular Formula C9H12O
Molecular Weight 136.191
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 3
Charge 0

SHOW SMILES / InChI
Structure of 2,4,6-NONATRIENAL, (2E,4E,6Z)-

SMILES

CC\C=C/C=C/C=C/C=O

InChI

InChIKey=XHDSWFFUGPJMMN-ZRGCPWHVSA-N
InChI=1S/C9H12O/c1-2-3-4-5-6-7-8-9-10/h3-9H,2H2,1H3/b4-3-,6-5+,8-7+

HIDE SMILES / InChI

Molecular Formula C9H12O
Molecular Weight 136.191
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 3
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Identification and formation of volatile components responsible for the characteristic aroma of mat rush (igusa).
2010
Analysis of 2,4,6-nonatrienal geometrical isomers from male flea beetles, Epitrix hirtipennis and E. fuscula.
2008-07-09
Male-produced aggregation pheromone compounds from the eggplant flea beetle (Epitrix fuscula): identification, synthesis, and field biossays.
2006-11
Characterization of the key aroma compounds in the beverage prepared from Darjeeling black tea: quantitative differences between tea leaves and infusion.
2006-02-08
Characterization of (E,E,Z)-2,4,6-nonatrienal as a character impact aroma compound of oat flakes.
2005-11-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:59:58 GMT 2025
Edited
by admin
on Mon Mar 31 20:59:58 GMT 2025
Record UNII
6791472F8N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4,6-NONATRIENAL, (2E,4E,6Z)-
Systematic Name English
FEMA NO. 4187, (2E,4E,6Z)-
Preferred Name English
2,4,6-NONATRIENAL, (E,E,Z)-
Systematic Name English
Code System Code Type Description
CAS
100113-52-8
Created by admin on Mon Mar 31 20:59:58 GMT 2025 , Edited by admin on Mon Mar 31 20:59:58 GMT 2025
PRIMARY
PUBCHEM
44256565
Created by admin on Mon Mar 31 20:59:58 GMT 2025 , Edited by admin on Mon Mar 31 20:59:58 GMT 2025
PRIMARY
FDA UNII
6791472F8N
Created by admin on Mon Mar 31 20:59:58 GMT 2025 , Edited by admin on Mon Mar 31 20:59:58 GMT 2025
PRIMARY