1134607-84-3

Basic information

• Product Name: (E)-N-benzyl-3,7-dimethylocta-2,6-dienamide
• Synonyms: (E)-N-benzyl-3,7-dimethylocta-2,6-dienamide
• CAS NO: 1134607-84-3
• Molecular Weight: 257.376
• Mol File: 1134607-84-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-N-benzyl-3,7-dimethylocta-2,6-dienamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-benzyl-3,7-dimethylocta-2,6-dienamide(1134607-84-3)
• EPA Substance Registry System: (E)-N-benzyl-3,7-dimethylocta-2,6-dienamide(1134607-84-3)

Safety Data

• Hazardous Substances Data: 1134607-84-3(Hazardous Substances Data)

Upstream product

• 106-24-1 Geraniol 
• 141-27-5 3,7-dimethyl-2,6-octadienal 
• 58558-13-7 (2E)-3,7-dimethyl-2,6-octadienoyl chloride 
• 100-46-9 benzylamine 
• 4698-08-2 (E)-geranic acid 

Relevant articles and documents

Synthesis and fungicidal activities of (Z/E)-3,7-dimethyl-2,6-octadienamide and its 6,7-epoxy analogues

In order to find new lead compounds with high fungicidal activity, (Z/E)-3,7-dimethyl- 2,6-octadienoic acids were synthesized via selective two-step oxidation using the commercially available geraniol/nerol as raw materials. Twenty-eight different (Z/E)-3,7-dimethyl-2,6-octadienamide derivatives were prepared by reactions of (Z/E)-carboxylic acid with various aromatic and aliphatic amines, followed by oxidation of peroxyacetic acid to afford their 6,7-epoxy analogues. All of the compounds were characterized by HR-ESI-MS and 1H-NMR spectral data. The preliminary bioassays showed that some of these compounds exhibited good fungicidal activities against Rhizoctonia solani (R. solani) at a concentration of 50 μg/mL. For example, 5C, 5I and 6b had 94.0%, 93.4% and 91.5% inhibition rates against R. solani, respectively. Compound 5f displayed EC50 values of 4.3 and 9.7 μM against Fusahum graminearum and R. Solani, respectively.