4205-06-5

Basic information

• Product Name: 2-(2-NITRO-PHENYL)-1H-IMIDAZOLE
• Synonyms: 2-(2-NITRO-PHENYL)-1H-IMIDAZOLE;1H-IMidazole,2-(2-nitrophenyl)-;2-(2-Nitrophenyl)iMidazole
• CAS NO: 4205-06-5
• Molecular Formula: C₉H₇N₃O₂
• Molecular Weight: 189.17078
• Mol File: 4205-06-5.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-NITRO-PHENYL)-1H-IMIDAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-NITRO-PHENYL)-1H-IMIDAZOLE(4205-06-5)
• EPA Substance Registry System: 2-(2-NITRO-PHENYL)-1H-IMIDAZOLE(4205-06-5)

Safety Data

• Hazardous Substances Data: 4205-06-5(Hazardous Substances Data)

Usage

General Description

2-(2-Nitro-phenyl)-1H-imidazole is a chemical compound that is also known as NITD609. It is an imidazole-based compound with a nitrophenyl group attached to the 2-position of the imidazole ring. 2-(2-NITRO-PHENYL)-1H-IMIDAZOLE has been studied for its potential pharmacological activities, including its antifungal and antiparasitic properties. It has shown promise as an inhibitor of various enzymes and has been investigated as a potential drug candidate for the treatment of various infectious diseases. Additionally, research has demonstrated its potential as an anti-cancer agent. However, further studies are needed to fully understand its mechanisms of action and potential therapeutic applications.

Upstream product

• 98-95-3 nitrobenzene 
• 50846-98-5 2-Diazo-2H-imidazole 
• 7664-93-9 sulfuric acid 
• 4405-13-4 glyoxal trimer dihydrate 
• 552-89-6 2-nitro-benzaldehyde 
• 288-32-4 1H-imidazole 
• 88-74-4 2-nitro-aniline 
• 131543-46-9 Glyoxal 

Downstream Products

• 29528-25-4 2-(2-aminophenyl)-1H-imidazole 
• 1160826-43-6 C₁₆H₁₀N₄O₅ 
• 1160826-50-5 C₁₆H₁₀BrN₃O₃ 
• 1327242-43-2 1-(4-nitrophenyl)-3-[2-(1H-imidazol-2-yl)phenyl]urea 
• 1327242-44-3 1-(4-nitrophenyl)-3-[2-(1H-imidazol-2-yl)phenyl]thiourea 
• 1327242-45-4 1-[3,5-bis(trifluoromethyl)phenyl]-3-[2-(1H-imidazol-2-yl)phenyl]urea 
• 1400866-34-3 C₁₇H₁₄N₄O₃ 
• 1400866-36-5 C₁₉H₁₈N₄O₃ 
• 1400866-37-6 C₁₈H₁₆N₄O₃ 
• 1400866-38-7 N-(2,4-dinitrophenyl)-2-(2-(2-nitrophenyl)-1H-imidazol-2-yl)propanamide 
• 1335144-93-8 C₁₅H₁₀N₄O₃ 

Relevant articles and documents

COMPOUNDS AND METHODS FOR TREATING CANCER

Substituted cinnamamide compounds and analogs, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or ameliorate cancer are provided.

Reactivity of hydroxy and amino derivatives of 2-phenyl-1H-imidazoline and 2-phenyl-1H-imidazole toward isocyanates: Synthesis of appropriate carbamates and ureas

Reactivity of 2-(4-hydroxyphenyl)-1H-imidazoline and 2-(4-hydroxyphenyl)- 1H-imidazole toward substituted phenyl isocyanates was studied. When mentioned imidazoline was treated with 2.5 equiv of substituted phenyl isocyanate, three N,O-dicarboxamides were

Clay-supported 2-phenyl-1H-imidazole derivatives for heterogeneous catalysis of Henry reaction

Figure represented. Six derivatives (1-6) of 2-phenyl-1H-imidazole were tested as catalysts of Henry reaction. Three new (4-6) 2-phenyl-1H-imidazole derivatives, differently substituted (thio)ureas, were synthesized and determined by 1H NMR and