cis-3-Hexenal

cis-3-Hexenal
Names
Preferred IUPAC name
(3Z)-Hex-3-enal
Other names
(Z)-Hex-3-enal
cis-3-Hexenal
Leaf aldehyde
Identifiers
6789-80-6
3D model (Jmol) Interactive image
ChEBI CHEBI:23292
ChemSpider 559032
ECHA InfoCard 100.027.141
PubChem 643941
UNII 6V54TKA96C
Properties
C6H10O
Molar mass 98.15 g·mol−1
Density 0.851 g/cm3
Boiling point 126 °C (259 °F; 399 K)
Related compounds
Related alkenals
Acrolein

Crotonaldehyde
(E,E)-2,4-Decadienal

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

cis-3-Hexenal, also known as (Z)-3-hexenal and leaf aldehyde, is colorless liquid and an aroma compound with an intense grassy-green odor of freshly cut green grass and leaves.[1][2] It is one of the major volatile compounds in ripe tomatoes. It is produced in small amounts by most plants and it acts as an attractant to many predatory insects. It is also a pheromone in many insect species.[3]

cis-3-Hexenal is an aldehyde. It is relatively unstable and isomerizes into the conjugated trans-2-hexenal. The related alcohol cis-3-hexen-1-ol is much more stable. It has a similar but weaker smell and is widely used in flavors and perfumes.

See also

References

  1. Molecule of the Month: Hexenal
  2. Hexenal / Chemistry World, Royal Society of Chemistry, 27 November 2013
  3. Pheromone database
This article is issued from Wikipedia - version of the 9/7/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.