1544-75-8

Basic information

• Product Name: 5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE
• Synonyms: 5-FLUORO-1,3-DIHYDROBENZOIMIDAZOL-2-ONE, 95+%;5-Fluoro-1,3-dihydrobenzoimidazol-2-one;5-fluoro-1,3-dihydro-2H-benzimidazol-2-one;2H-BenziMidazol-2-one, 5-fluoro-1,3-dihydro-;5-Fluoro-1H-benzo[d]iMidazol-2(3H)-one;5-Fluoro-1H-benzo[d]imidazol-2(3H);5-FLUOROBENZIMIDAZOLONE;5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE
• CAS NO: 1544-75-8
• Molecular Formula: C₇H₅FN₂O
• Molecular Weight: 152.13
• EINECS: 200-258-5
• Product Categories: BENZIMIDAZOLE
• Mol File: 1544-75-8.mol
• Article Data: 24

Chemical Properties

• Melting Point: 300 °C
• Boiling Point: 118.83 °C at 760 mmHg
• Flash Point: 25.668 °C
• Appearance: /
• Density: 1.367 g/cm³
• Vapor Pressure: 16.381mmHg at 25°C
• Refractive Index: 1.561
• Storage Temp.: 2-8°C
• PKA: 11.00±0.30(Predicted)
• CAS DataBase Reference: 5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE(1544-75-8)
• EPA Substance Registry System: 5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE(1544-75-8)

Safety Data

• Hazardous Substances Data: 1544-75-8(Hazardous Substances Data)

Usage

General Description

5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE is a chemical compound with the molecular formula C7H6FN3O. It is a benzimidazole derivative with a fluorine atom attached to the carbon-5 position. 5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE has been studied for its potential pharmacological properties, including its use as an anti-tumor and anti-cancer agent. Its structure and properties make it a valuable tool for medicinal chemistry research and drug development. 5-FLUORO-1,3-DIHYDRO-BENZIMIDAZOL-2-ONE has potential applications in the development of new drugs and therapies for various medical conditions.

InChI:InChI=1/C7H5FN2O/c8-4-1-2-5-6(3-4)10-7(11)9-5/h1-3H,(H2,9,10,11)

Upstream product

• 367-31-7 4-fluoro-1,2-phenylenediamine 
• 503-38-8 trichloromethyl chloroformate 
• 319-03-9 4-fluorophthalic anhydride 
• 1202680-24-7 phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate 
• 530-62-1 1,1'-carbonyldiimidazole 
• 75-44-5 phosgene 
• 124-38-9 carbon dioxide 

Downstream Products

• 401567-12-2 2-chloro-5-fluoro-1-methyl-1H-benzimidazole 
• 1073558-68-5 8-(5-fluoro-1H-benzimidazol-2-yl)-3-phenyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one 
• 4857-06-1 2-chloro-1H-benzoimidazole 

Relevant articles and documents

A bifunctional tungstate catalyst for chemical fixation of CO2 at atmospheric pressure

No pressure: A simple monomeric tungstate, [WO4]2-, serves as a highly efficient homogeneous catalyst for various transformations of CO2 at atmospheric pressure. The tungsten-oxo moiety activates CO2 and the substrate simultaneously. The catalyst system is high yielding and applicable to a wide range of substrates such as amines (see scheme), 2-aminobenzonitriles, and propargylic alcohols. Copyright

CdSnO3/SnD NPs as a Nanocatalyst for Carbonylation of o-Phenylenediamine with CO2

In order to carbonize o-phenylenediamine with CO2, an effective approach was used with UV light irradiation by Sn(IV) doping DFNS (SnD) supported CdSnO3 as a catalyst (CdSnO3/SnD). In this catalyst, SnD with the ratios of Si/Sn in the range of 6 to 50 were obtained using the Direct Hydrothermal Synthesis (DHS), and the nanoparticles of CdSnO3 on the surfaces of SnD were reduced in situ. Scanning Electron Microscope (SEM), X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray Energy Dispersive Spectroscopy (EDS), and Transmission Electron Microscopy (TEM) were utilized for characterizing CdSnO3/SnD. It was found that CdSnO3/SnD nanostructures could be used for synthesizing o-phenylenediamines due to their effective and novel catalytic behavior through the reaction between o-phenylenediamines and CO2. Graphic Abstract: [Figure not available: see fulltext.]

1,3-dimethyl benzimidazolones are potent, selective inhibitors of the brpf1 bromodomain

The BRPF (bromodomain and PHD finger-containing) protein family are important scaffolding proteins for assembly of MYST histone acetyltransferase complexes. Here, we report the discovery, binding mode, and structure-activity relationship (SAR) of the firs

SBA-15 Supported Dendritic ILs as a Green Catalysts for Synthesis of 2-Imidazolidinone from Ethylenediamine and Carbon Dioxide

In this work, a simple and facile approach is conducted for preparing many new SBA-15 supported dendritic imidazolium ILs heterogeneous catalysts SBA-15/IL(1–3) having high ionic density from SBA-15. SBA-15/IL(3) as a green heterogeneous catalyst can be used for synthesis of 2-imidazolidinone from ethylenediamine and carbon dioxide and considering solvent-free condition. SBA-15/IL(3) showed to have the highest catalytic activity besides a positive dendritic influence on the yields of the synthesis of 2-imidazolidinone in the presence of CO2 is seen because of existing the high-density peripheral zwitterionic ionic liquid functional groups on the biobased SBA-15/IL(3) catalyst surfaces. Graphical Abstract: [Figure not available: see fulltext.]

Application of sea urchin-shaped cobalt-based photocatalyst in synthesis of benzoazacycle by converting CO2

The invention relates to the technical field of photocatalysis, in particular to application of a sea urchin-shaped cobalt-based photocatalyst to synthesis of benzoazacycle by converting CO2. A complex is of a sea urchin-shaped microsphere structure, which is composed of an organic ligand L and cobalt nitrate hexahydrate and is formed by arranging a plurality of nano needle-shaped complex crystals. The main body of the organic ligand L is p-aminobenzoic acid; the application comprises the following steps: introducing CO2 into a solution containing o-phenylenediamine compounds, carrying out carbonylation reaction and cyclization with o-phenylenediamine compounds under the action of the urchin-shaped cobalt-based catalyst to generate the benzoazacycle compounds. The sea urchin-shaped microsphere structure cobalt-based catalyst formed by the obtained nano needle-shaped complex crystal has a very large specific surface area and high photocatalytic efficiency; when the photocatalyst is adopted to catalyze and activate CO2, the reaction for synthesizing the benzoazacycle by converting CO2 can be carried out at room temperature, so that the energy consumption is greatly reduced, and the cost is reduced.