85770-95-2

Usage

Uses

Used in Organic Synthesis:
BIS(1H-BENZO[D]IMIDAZOL-2-YLTHIO)METHANE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, contributing to the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Research:
BIS(1H-BENZO[D]IMIDAZOL-2-YLTHIO)METHANE is used as a starting material or building block in the design and synthesis of new drugs. Its potential biological activities and compatibility with various pharmacophores make it an attractive target for drug discovery and development.
Used in Drug Development:
BIS(1H-BENZO[D]IMIDAZOL-2-YLTHIO)METHANE is used as a potential active pharmaceutical ingredient (API) in the development of new drugs. Its unique properties and potential biological activities suggest that it may have therapeutic effects against various diseases and conditions, warranting further investigation in medicinal chemistry.
Used in Material Science:
BIS(1H-BENZO[D]IMIDAZOL-2-YLTHIO)METHANE is used as a component in the development of new materials with specific properties. Its unique structure and chemical reactivity can contribute to the creation of advanced materials for various applications, such as sensors, catalysts, or functional coatings.

Upstream product

• 583-39-1 2,3-dihydrobenzimidazol-2-thione 
• 74-95-3 1,1-dibromomethane 
• 75-09-2 dichloromethane 
• 134469-07-1 Benzimidazol-2-thiol 
• 58536-70-2 benzimidazole-2-thione 

Relevant academic research and scientific papers

Computational, MD simulation, SEM/EDX and experimental studies for understanding adsorption of benzimidazole derivatives as corrosion inhibitors in 1.0 M HCl solution

The adsorption and corrosion inhibition performance of two benzimidazole derivatives, namely:2-(allylthio)-1H-benzo[d]imidazole (SHA) and bis((1H-benzo[d]imidazole-2-yl)thio)methane (BB1C) were studied as a corrosion inhibitors for mild steel (MS) in 1.0 M HCl solution using Weight Loss (WL) measurements, Potentiodynamic Polarization (PDP), Electrochemical Impedance Spectroscopy (EIS), Scanning Electron Microscopy(SEM) and Energy Dispersive X-ray (EDX) analysis. The kinetics of corrosion retardation were inspected by polarization studies, and the respective achievements declared that both compounds could retard corrosion reactions via cathodic/anodic (mixed) inhibition mechanism. The adsorption process on MS surface obeyed Langmuir isotherm. Adsorption and thermodynamic parameters were also evaluated. SEM/EDX analysis strongly supports the obtained results and confirms the existence of a barrier film on the metal surface. Our findings provide deeper insights into understanding the interaction mechanisms of SHA and BB1C with MS surface. Experimental outcomes support the outcomes obtained from DFT and Molecular dynamic (MD) simulation.

Synthesis and crystal structures of some bis-benzimidazoles, -benzothiazoles and -benzoxazoles by an alternative route: Their complexation with copper(II) salts

A novel and convenient synthetic route towards new bis-benzimidazoles, -benzothiazoles and -benzoxazoles from readily available starting materials has been established. These compounds have thioethers at the 2 position of the heterocycle and the resultant

Infrared vibrations of carbon-sulphur bonds in bis(benzoxazole-, benzoimidazole-benzothiazole-2-thiol)methane. Assignments by "selenation"

The i.r. spectra of the title compounds have been compared with those of the corresponding-2-selenol derivatives.The i.r. vibrational assignments of the thioether links have been made on the basis of the selenation.The moiety CH2-(Y-CH2)2 (Y = S, Se) present in all the compounds considered gives typical absorptions in the fingerprint region.