165901-26-8

Basic information

• Product Name: 1H-IMidazole, 2-(4-fluorophenyl)-4,5-dihydro-
• Synonyms: 1H-IMidazole, 2-(4-fluorophenyl)-4,5-dihydro-;4,5-dihydro-2-(2,4,6-trimethylphenyl)-1H-Imidazole
• CAS NO: 165901-26-8
• Molecular Formula: C₉H₉FN₂
• Molecular Weight: 164.1795632
• Mol File: 165901-26-8.mol
• Article Data: 14

Chemical Properties

• Melting Point: 153 °C(Solv: cyclohexane (110-82-7))
• Boiling Point: 243.7±42.0 °C(Predicted)
• Appearance: /
• Density: 1.23±0.1 g/cm3(Predicted)
• PKA: 9.87±0.40(Predicted)
• CAS DataBase Reference: 1H-IMidazole, 2-(4-fluorophenyl)-4,5-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-IMidazole, 2-(4-fluorophenyl)-4,5-dihydro-(165901-26-8)
• EPA Substance Registry System: 1H-IMidazole, 2-(4-fluorophenyl)-4,5-dihydro-(165901-26-8)

Safety Data

• Hazardous Substances Data: 165901-26-8(Hazardous Substances Data)

Usage

General Description

1H-IMidazole, 2-(4-fluorophenyl)-4,5-dihydro- is a chemical compound with the molecular formula C9H9FN2. It is a derivative of imidazole with a 4-fluorophenyl group attached to the 2-position, resulting in a 4,5-dihydro structure. 1H-IMidazole, 2-(4-fluorophenyl)-4,5-dihydro- is used in pharmaceutical research and drug development, particularly in the synthesis of potential antifungal and antimicrobial agents. Additionally, it may also have applications in the field of agricultural chemistry. The specific properties and uses of this chemical compound are the subject of ongoing research and development efforts in various scientific disciplines.

Upstream product

• 1194-02-1 4-fluorobenzonitrile 
• 107-15-3 ethylenediamine 
• 42202-95-9 4-fluoro-N-hydroxybenzimidoyl chloride 
• 403-33-8 methyl 4-flurobenzoate 
• 22179-72-2 4-fluorothiobenzamide 
• 7119-23-5 2-Brom-3,3,3-trifluor-1-(4-fluorphenyl)-prop-1-en 
• 459-57-4 4-fluorobenzaldehyde 
• 766-98-3 1-ethynyl-4-fluorobenzene 
• 98-88-4 benzoyl chloride 
• 39833-45-9 3-(4-fluorophenyl)-1-phenylprop-2-yn-1-one 

Downstream Products

• 4278-08-4 2-(4-fluorophenyl)-1H-imidazole 
• 1441929-83-4 C₁₅H₁₃FN₄O₂ 
• 1441932-03-1 C₁₅H₁₅FN₄ 
• 1621586-60-4 2-(4-fluorophenyl)-1-(4-(methylsulfonyl)phenyl)-4,5-dihydro-1H-imidazole 
• 1621586-72-8 4-(2-(4-fluorophenyl)-4,5-dihydroimidazol-1-yl)benzenesulfonamide 

Relevant articles and documents

Benzamidine derivatives, preparation methods and applications

The present invention discloses benzamidine derivatives, preparation methods and applications. Benzamidine derivatives involved include benzamidine derivatives containing 1,2,4-triazole methyl and non-heterocyclically substituted benzamidine derivatives.

New Insights into the Role of Imidazolium-Based Promoters for the Electroreduction of CO2 on a Silver Electrode

The electrochemical reduction of CO2 to CO is a reaction of central importance for sustainable energy conversion and storage. Herein, structure-activity relationships of a series of imidazolium-based cocatalysts for this reaction are described,

Efficient synthesis of 2-imidazolines in the presence of molecular iodine under ultrasound irradiation

An efficient one-pot synthesis process for preparing 2-imidazolines from aldehydes and ethylenediamine using molecular iodine and potassium carbonate in absolute ethanol at 25-30°C under ultrasound irradiation is described. The synthetic strategy has the following advantages: mild conditions and low costs requirements, readily available catalyst, short reaction times, simplicity of operation, and good-to-excellent yields.