1807-54-1

Usage

Uses

Used in Synthetic Organic Chemistry:
Hydrazine, tetrakis(4-methoxyphenyl)is used as a reducing agent for the synthesis of pharmaceuticals and agrochemicals. Its reducing properties enable the conversion of various functional groups, facilitating the production of desired compounds in the synthesis process.
Used in Coordination Chemistry:
Hydrazine, tetrakis(4-methoxyphenyl)is used as a ligand for forming complexes with various metal ions. Its ability to chelate metal ions allows for the creation of stable complexes with unique properties, which can be utilized in various applications, such as catalysis and material science.
Used in Pharmaceutical Industry:
Hydrazine, tetrakis(4-methoxyphenyl)is used as a key intermediate in the synthesis of certain pharmaceutical compounds. Its presence in the molecular structure can contribute to the biological activity and therapeutic effects of the final drug product.
Used in Agrochemical Industry:
Hydrazine, tetrakis(4-methoxyphenyl)is used in the synthesis of agrochemicals, such as pesticides and herbicides. Its role in the production process helps to create effective compounds for controlling pests and weeds in agricultural settings.

Upstream product

• 101-70-2 bis(4-methoxyphenyl)amine 
• 60-29-7 diethyl ether 

Downstream Products

• 6947-36-0 N-nitrosodi(anisyl)amine 
• 101-70-2 bis(4-methoxyphenyl)amine 
• 31438-43-4 2,7-dimethoxy-5,10-bis-(4-methoxy-phenyl)-5,10-dihydro-phenazine 
• 2643-00-7 di-p-anisylnitroxide 

Relevant academic research and scientific papers

Bismuth Amides Mediate Facile and Highly Selective Pn–Pn Radical-Coupling Reactions (Pn=N, P, As)

The controlled release of well-defined radical species under mild conditions for subsequent use in selective reactions is an important and challenging task in synthetic chemistry. We show here that simple bismuth amide species [Bi(NAr2)3] readily release aminyl radicals [NAr2]. at ambient temperature in solution. These reactions yield the corresponding hydrazines, Ar2N?NAr2, as a result of highly selective N?N coupling. The exploitation of facile homolytic Bi?Pn bond cleavage for Pn?Pn bond formation was extended to higher homologues of the pnictogens (Pn=N–As): homoleptic bismuth amides mediate the highly selective dehydrocoupling of HPnR2 to give R2Pn?PnR2. Analyses by NMR and EPR spectroscopy, single-crystal X-ray diffraction, and DFT calculations reveal low Bi?N homolytic bond-dissociation energies, suggest radical coupling in the coordination sphere of bismuth, and reveal electronic and steric parameters as effective tools to control these reactions.

An electrospray ionization source for the investigation of thermally initiated reactions

An electrospray ionization source for mass spectrometry is described, which allows one to heat the spray capillary. Thermal dissociation of the trityl dimer 1 and tetra(p-anisyl)hydrazine (3) have been investigated, operating the ESI source as electrolyti

Kinetics of Oxidation of Unsubstituted and Substituted Diphenylamines by Alkaline Hexacyanoferrate(III)

Oxidation of unsubstituted and substituted diphenylamines by alkaline hexacyanoferrate(III) at constant ionic strength in aqueous methanol is first order each in and , and independent of in the range studied.The Hammet plot y