56797-44-5

Basic information

• Product Name: 8,11,14-Heptadecatrienal, (8Z,11Z,14Z)-
• Synonyms: heptadeca-8c,11c,14c-trienal;norlinolenic aldehyde;(8Z,11Z,14Z)-heptadecatrienal;(Z,Z,Z)-8,11,14-heptadecatrienal;norlinolenaldehyde
• CAS NO: 56797-44-5
• Molecular Formula: C17H28O
• Molecular Weight: 248.40400
• Mol File: 56797-44-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 352.7±21.0 °C(Predicted)
• Density: 0.864±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 8,11,14-Heptadecatrienal, (8Z,11Z,14Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 8,11,14-Heptadecatrienal, (8Z,11Z,14Z)-(56797-44-5)
• EPA Substance Registry System: 8,11,14-Heptadecatrienal, (8Z,11Z,14Z)-(56797-44-5)

Safety Data

• Hazardous Substances Data: 56797-44-5(Hazardous Substances Data)

Upstream product

• 463-40-1 (9Z,12Z,15Z)-octadeca-9-12,15-trienoic acid 
• 155273-06-6 (9Z,12Z,15Z)-Octadeca-9,12,15-triene-1,2-diol 
• 133585-84-9 (8Z,11Z,14Z)-8,11,14-heptadecatrien-1-ol 
• 878288-02-9 8,11,14-heptadecatriyn-1-ol 
• 10160-25-5 7-bromo-1-(2-tetrahydropyranyloxy)heptane 
• 10160-26-6 9-(2-tetrahydropyranyloxy)-1-nonyne 
• 10160-24-4 7-bromoheptyl alcohol 
• 629-30-1 1,7-heptandiol 
• 16400-32-1 1-bromo-pent-2-yne 
• 35378-76-8 octa-2,5-diyn-1-ol 
• 1558-79-8 2,5-octadiynyl bromide 
• 117606-23-2 2,5-octadiyn-1-ol tetrahydropyranyl ether 
• 155273-04-4 methyl α-hydroxy linolenate 

Relevant articles and documents

Enzymatic formation of unsaturated long chain fatty aldehydes in Ulva pertusa

(Z)-8-Heptadecenal, (Z,Z)-8, 11-heptadecadienal and 8,11,14-heptadecatrienal, were produced enzymatically from oleic, linoleic and linoleni.

Abnormal Catabolites of Unsaturated Fatty Acids by In Vitro Reaction of Crude Enzyme from Infected Higher Plants

The reaction of α-linolenic acid with crude enzyme (lipoxygenase) obtained from infected pumpkins led to the formation of 8Z,11Z,14Z-heptadecatrienal (noraldehyde) and its acid (noracid) in addition to 13S-hyroperoxy linolenic acid.Since the noraldehyde and its acid were also isolated from the crude enzyme reaction of other infected plants, their formation seems to be related with the pathogen-infection of higher plants.