5347-97-7

Basic information

• Product Name: 2-{(E)-amino[(2E)-(2-methoxybenzylidene)hydrazinylidene]methyl}-1-hydroxy-1-oxohydrazinium
• CAS NO: 5347-97-7
• Molecular Formula: C₉H₁₁N₅O₃
• Molecular Weight: 238.2227
• Mol File: 5347-97-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-{(E)-amino[(2E)-(2-methoxybenzylidene)hydrazinylidene]methyl}-1-hydroxy-1-oxohydrazinium(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{(E)-amino[(2E)-(2-methoxybenzylidene)hydrazinylidene]methyl}-1-hydroxy-1-oxohydrazinium(5347-97-7)
• EPA Substance Registry System: 2-{(E)-amino[(2E)-(2-methoxybenzylidene)hydrazinylidene]methyl}-1-hydroxy-1-oxohydrazinium(5347-97-7)

Safety Data

• Hazardous Substances Data: 5347-97-7(Hazardous Substances Data)

Usage

Structure

Contains a hydrazine group and a methoxybenzylidene group

Derivative

Hydroxy hydrazinium, with a hydroxyl group and a hydrazine group

Functional groups

Amine group and oxo group

Potential applications

Pharmaceuticals, organic synthesis, and materials science

Research

Further studies are needed to fully understand its properties and potential uses

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 18264-75-0 3-amino-1-nitroguanidine 
• 18264-75-0 1-amino-2-nitroguanidine 

Relevant articles and documents

Synthesis, insecticidal and fungicidal activities of methyl 2-(methoxyimino)-2-(2-((1-(N′-nitrocarbamimidoyl)-2-hydrocarbylidene-hydrazinyl)methyl)phenyl)acetates

N′-Nitro-2-hydrocarbylidenehydrazinecarboximidamides and methoxyacrylates are two types of important agrochemicals. By combining their key fragments into one framework, a series of the title compounds was designed and synthesized. Some of these compounds have shown excellent insecticidal activities for aphides, for example, the LC50 values of compounds 6-06, 6-11 and 6-19 against M. perslcae and H. amygdale were found to be 1.9/14.4, 13.4/1.5 and 0.3/38.4 mg L-1 respectively. They were also effective against the mycelium growth of B. cinerea in vitro. Compound 6-04 could control (～100%) cucumber anthrax and rice blast at 100 mg L-1 in vivo, and inhibit the spore germination (～100%) of vegetable gray mold at 6.25 mg L-1. These compounds could be considered as potential insecticidal or fungicidal candidates for crop protection. The results of structure-activity relationship (SAR) studies are discussed.