870450-93-4

Basic information

• Product Name: 1-(4-TRIFLUOROMETHYLPHENYL)-1H-BENZOIMIDAZOLE
• Synonyms: 1-(4-TRIFLUOROMETHYLPHENYL)-1H-BENZOIMIDAZOLE
• CAS NO: 870450-93-4
• Molecular Formula: C14H9F3N2
• Molecular Weight: 262.23
• Product Categories: pharmacetical
• Mol File: 870450-93-4.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 359.585 °C at 760 mmHg
• Flash Point: 171.271 °C
• Appearance: /
• Density: 1.298g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.573
• CAS DataBase Reference: 1-(4-TRIFLUOROMETHYLPHENYL)-1H-BENZOIMIDAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-TRIFLUOROMETHYLPHENYL)-1H-BENZOIMIDAZOLE(870450-93-4)
• EPA Substance Registry System: 1-(4-TRIFLUOROMETHYLPHENYL)-1H-BENZOIMIDAZOLE(870450-93-4)

Safety Data

• Hazardous Substances Data: 870450-93-4(Hazardous Substances Data)

Usage

General Description

1-(4-Trifluoromethylphenyl)-1H-benzoimidazole is a chemical compound with a molecular formula C14H9F3N2. It is a benzimidazole derivative, which is a class of organic compounds containing a fused benzene and imidazole ring. 1-(4-TRIFLUOROMETHYLPHENYL)-1H-BENZOIMIDAZOLE is characterized by a trifluoromethyl group attached to the phenyl ring, which imparts unique chemical properties such as increased lipophilicity and electron-withdrawing effects. It is commonly used in pharmaceutical research and drug development due to its potential biological activities, including antitumor, antifungal, and antiviral properties. The compound's structural features make it a valuable synthetic building block for the development of new drug candidates targeting various diseases.

InChI:InChI=1/C14H9F3N2/c15-14(16,17)10-5-7-11(8-6-10)19-9-18-12-3-1-2-4-13(12)19/h1-9H

Upstream product

• 51-17-2 benzoimidazole 
• 98-56-6 4-chlorobenzotrifluoride 
• 128796-39-4 4-trifluoromethylphenylboronic acid 
• 455-13-0 4-Iodobenzotrifluoride 
• 214360-65-3 4-trifluoromethylphenylboronic acid pinacol ester 
• 402-43-7 p-trifluoromethylphenyl bromide 

Downstream Products

• 947417-54-1 3-methyl-1-(4-(trifluoromethyl)phenyl)benzoimidazolium iodide 

Relevant articles and documents

Dynamic Kinetic Sensitization of β-Dicarbonyl Compounds—Access to Medium-Sized Rings by De Mayo-Type Ring Expansion

Herein, we present a photocatalyzed two-carbon ring expansion of β-dicarbonyl compounds with unactivated olefins that provides facile access to medium-sized rings. Selective sensitization of the substoichiometric enol tautomer enables reactivity of substr

Efficient NIR electrochemiluminescent dyes based on ruthenium(ii) complexes containing an N-heterocyclic carbene ligand

Three new ruthenium(ii) complexes containing an N-heterocyclic carbene (NHC) ligand (RuNHC) have been successfully synthesized and proved to be efficient near-infrared (NIR) ECL (electrogenerated chemiluminescence) luminophores. In addition to the advanta

Green synthesis of CuO nanoflakes from copper pincer complex for effective N-arylation of benzimidazole

Nanostructured CuO is synthesized in water using copper pincer complex as precursor without any stabilizing agent and characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-