1325765-39-6

Basic information

• Product Name: C₉H₁₀FN₅O₂
• Synonyms: C₉H₁₀FN₅O₂
• CAS NO: 1325765-39-6
• Molecular Weight: 239.209
• Mol File: 1325765-39-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₉H₁₀FN₅O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₉H₁₀FN₅O₂(1325765-39-6)
• EPA Substance Registry System: C₉H₁₀FN₅O₂(1325765-39-6)

Safety Data

• Hazardous Substances Data: 1325765-39-6(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 556-88-7 2-nitroguanidine 
• 371-40-4 4-fluoroaniline 
• 2146-07-8 p-fluoroaniline hydrochloride 
• 1325765-37-4 C₇H₆FN*ClH 

Downstream Products

• 1200835-75-1 1-((6-chloropyridin-3-yl)methyl)-5-(4-fluorophenyl)-1,3,5-hexahydrotriazine-2-(N-nitro)imine 
• 1200835-82-0 1-((2-chlorothiazol-5-yl)methyl)-5-(4-fluorophenyl)-1,3,5-hexahydrotriazine-2-(N-nitro)imine 

Relevant articles and documents

Novel (E)-β-farnesene analogues containing 2-nitroiminohexahydro-1,3,5-triazine: Synthesis and biological activity evaluation

In order to discover novel eco-friendly compounds with good activity for aphid control, (E)-β-farnesene (EβF), the main component of the aphid alarm pheromone, was chosen as the lead compound. By introducing a 2-nitroimino-hexahydro-1,3,5-triazine moiety (abbreviated NHT) to replace the unstable conjugated double bond system of EβF, a series of novel EβF analogues containing the NHT moiety were synthesized via the reaction of substituted NHT rings with (E)-1-chloro-3,7-dimethylocta-2,6-diene. All the compounds were characterized by 1H-NMR, 13C-NMR, IR, and high resolution mass spectroscopy (HRMS). The bioassay results showed that all the analogues displayed different repellent and aphicidal activities against green peach aphid (Myzus persicae). Particularly, the analogue 4r exhibited obvious repellent activity (repellent proportion: 78.43%) and similar aphicidal activity against M. persicae (mortality: 82.05%) as the commercial compound pymetrozine (80.07%). A preliminary structure-activity relationship (SAR) study was also performed, which offered valuable clues for the design of further new EβF analogues.