67082-03-5

Basic information

• Product Name: 2-[(E)-amino{2-[(E)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazinylidene}methyl]-1-hydroxy-1-oxohydrazinium
• CAS NO: 67082-03-5
• Molecular Formula: C₈H₉N₅O₃
• Molecular Weight: 224.1962
• Mol File: 67082-03-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-[(E)-amino{2-[(E)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazinylidene}methyl]-1-hydroxy-1-oxohydrazinium(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(E)-amino{2-[(E)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazinylidene}methyl]-1-hydroxy-1-oxohydrazinium(67082-03-5)
• EPA Substance Registry System: 2-[(E)-amino{2-[(E)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazinylidene}methyl]-1-hydroxy-1-oxohydrazinium(67082-03-5)

Safety Data

• Hazardous Substances Data: 67082-03-5(Hazardous Substances Data)

Usage

Structure

2-[(E)-amino2-[(E)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazinylidenemethyl]-1-hydroxy-1-oxohydrazinium

Properties

Antiseptic, antibacterial

Function

Disrupts bacterial DNA function, causing cell death

Uses

Topical antiseptic for minor cuts, burns, and infections; disinfectant for medical instruments; treatment of certain skin conditions and infections in combination with other medications

Precautions

Can cause skin irritation and allergic reactions in some individuals

Upstream product

• 90-02-8 salicylaldehyde 
• 18264-75-0 3-amino-1-nitroguanidine 
• 18264-75-0 1-amino-2-nitroguanidine 

Downstream Products

• 90-02-8 salicylaldehyde 

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.