1335128-30-7

Basic information

• Product Name: C₁₀H₁₃N₃O₂
• CAS NO: 1335128-30-7
• Molecular Weight: 207.232
• Mol File: 1335128-30-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₀H₁₃N₃O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₀H₁₃N₃O₂(1335128-30-7)
• EPA Substance Registry System: C₁₀H₁₃N₃O₂(1335128-30-7)

Safety Data

• Hazardous Substances Data: 1335128-30-7(Hazardous Substances Data)

Upstream product

• 121-33-5 vanillin 
• 120-25-2 4-ethoxy-3-methoxybenzaldehyde 
• 61813-58-9 (4-ethoxy-3-methoxyphenyl)methanol 
• 155583-43-0 4-ethoxy-3-methoxybenzyl bromide 

Downstream Products

• 1335128-34-1 4-((4-chlorophenyl)(hydroxyl)methyl)-1-(3-methoxy-4-ethoxybenzyl)-1H-1,2,3-triazole 

Relevant articles and documents

Synthesis and biological evaluation of isosteric analogs of mandipropamid for the control of oomycete pathogens

A series of isosteric analogs of mandipropamid were designed and synthesized via 'click chemistry'. The amide bond of mandipropamid was substituted by a 1,2,3-triazole functional group. The bioassay results have indicated that some of the title compounds exhibited moderate fungicidal activity against Pseudoperonospora cubensis, and the activity has been systematically studied as a function of molecular structure. The low activity of the mandipropamid analog that contains a lipid chain is likely due to the presence of a weak hydrogen bond donor in the 1,2,3-triazole. Furthermore, we have performed the molecular modeling and found that N-methylamide could be more effective than amide as the surrogates to 1,2,3-triazole, which ultimately leads to a longer distance (1.1A longer) between the two substitutes in the 1,4-disubstituted 1,2,3-triazole compound.