17433-92-0

Basic information

• Product Name: Hydrazinecarboxamide, N-(3-nitrophenyl)-
• CAS NO: 17433-92-0
• Molecular Formula: C7H8N4O3
• Molecular Weight: 196.166
• Mol File: 17433-92-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Hydrazinecarboxamide, N-(3-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarboxamide, N-(3-nitrophenyl)-(17433-92-0)
• EPA Substance Registry System: Hydrazinecarboxamide, N-(3-nitrophenyl)-(17433-92-0)

Safety Data

• Hazardous Substances Data: 17433-92-0(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 13142-61-5 (3-nitro-phenyl)-urea 
• 7803-57-8 hydrazine hydrate 
• 50699-52-0 (3-nitro-phenyl)-carbamic acid phenyl ester 
• 51028-37-6 (3-nitro-phenyl)-carbamoyl chloride 
• 3532-31-8 3-nitrobenzoyl azide 
• 3320-87-4 isocyanic acid (3-nitro-phenyl) ester 
• 6275-72-5 ethyl N-(m-nitrophenyl)carbamate 

Relevant articles and documents

Azobenzene-Semicarbazone Enables Optical Control of Insect Sodium Channels and Behavior

Photopharmacology uses molecular photoswitches to establish control over the action of bioactive molecules. The application of photopharmacology in the research of invertebrate sodium channels has not been investigated. Here we report several photochromic ligands of metaflumizone. One ligand, termed ABM04, underwent reversible trans-cis isomerization under ultraviolet or blue light irradiation. cis-ABM04 had excellent larvicidal activity against mosquito larvae with an LC50 value of 4.39 μM and showed insecticidal activity against Mythimna separata with an LC50 value of 7.19 μM. However, trans-ABM04 was not found to have biological activity. ABM04 (10 μM) can induce depolarization of dorsal unpaired median neurons and enable the real-time photoregulation of mosquito larval behavior. The precise regulation of invertebrate sodium channels is realized for the first time, which provides a new strategy for the basic and accurate research of invertebrate sodium channels.