37494-06-7

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1,1'-(methylenedi-4,1-phenylene)bis[2-chlorois used as an intermediate in the synthesis of various pharmaceuticals for its reactive chemical properties. It aids in the production of drugs with specific therapeutic effects.
Used in Pesticide Industry:
Ethanone, 1,1'-(methylenedi-4,1-phenylene)bis[2-chlorois utilized in the formulation of pesticides due to its reactivity and ability to act as an effective agent against pests. Its strong chlorine content contributes to its pesticidal properties.
Used in Dye Industry:
Ethanone, 1,1'-(methylenedi-4,1-phenylene)bis[2-chlorois employed in the production of dyes because of its potential to impart color to various materials. Its chemical structure allows it to be integrated into dye molecules, enhancing their colorfastness and performance.
Safety Precautions:
Given its classification as a hazardous substance, proper safety measures should be taken when handling Ethanone, 1,1'-(methylenedi-4,1-phenylene)bis[2-chloro-. This includes using personal protective equipment, ensuring proper ventilation, and following guidelines to prevent harmful exposure through ingestion or inhalation.

Upstream product

• 101-81-5 Diphenylmethane 
• 79-04-9 chloroacetyl chloride 

Downstream Products

• 93408-24-3 4,4'-di(1-hydroxy-2-chloroethyl)-diphenyl methane 
• 17755-58-7 4,4'-Methylen-bis(phenylglyoxylohydroxamoylchlorid) 
• 89302-44-3 2,2'-(methylenedi-1,4-phenylene)bis<2-hydroxy-4,4-dimethylmorpholinium> dichloride 
• 103042-06-4 bis-(4-iodoacetyl-phenyl)-methane 
• 110008-20-3 bis-(4-acetoxyacetyl-phenyl)-methane 

Relevant academic research and scientific papers

The b, butyrylcholinesterase with double-inhibiting active compound

The invention provides an inhibitor of acetylcholine esterase and cholinesterase shown in the general formula (I), wherein R1, R2 and N form an aliphatic heterocyclic ring with 3-7 carbons containing 1-2 hetero atoms, and X is selected from a covalent bon

Synthesis of (2-hydroxo-5-chlorophenylaminoisonitrosoacetyl)phenyl ligands and their complexes: Spectral, thermal and solvent-extraction studies

Four different types of new ligands Ar[COC(NOH)R] n (Ar=biphenyl, n = 1 H2L1; Ar=biphenyl, n = 2 H 4L2; Ar=diphenylmethane, n = 1 H2L3; Ar=diphenylmethane, n = 2 H4L4; R=2-amino-4-chlorophenol in all ligands) have been obtained from 1 equivalent of chloroketooximes Ar[COC(NOH)Cl] n (HL1-H2L4) and 1 equivalent of 2-amino-4-chlorophenol (for H2L1 and H 2L3) or 2 equivalent of 2-amino-4-chlorophenol (for H 4L2 and H4L4). (Mononuclear or binuclear cobalt(II), nickel(II), copper(II) and zinc(II) complexes were synthesized with these ligands.) These compounds have been characterized by elemental analyses, AAS, infra-red spectra and magnetic susceptibility measurements. The ligands have been further characterized by 1H NMR. The results suggest that the dinuclear complexes of H2L1 and H2L3 have a metal:ligand ratio of 1:2; the mononuclear complexes of H4L2 and H4L4 have a metal:ligand ratio of 1:1 and dinuclear complexes H4L2 and H4L4 have a metal:ligand ratio of 2:1. The binding properties of the ligands towards selected transition metal ions (Mn II, CoII, NiII, CuII, Zn II, PbII, CdII, HgII) have been established by extraction experiments. The ligands show strong binding ability towards mercury(II) ion. In addition, the thermal decomposition of some complexes is studied in nitrogen atmosphere.

Method of producing ethynyl aromatic compounds

The process of producing ethynyl aromatic compounds which are useful as intermediates in the preparation of 3-dimensional carbon-carbon structures for aerospace and military applications and as starting materials in the preparation of organic semi-conduct