3911-49-7

Usage

Uses

Used in Organic Synthesis:
(4-nitrophenyl)(diphenyl)methanol is used as a building block for the preparation of various pharmaceutical and agrochemical compounds due to its unique structure and functional groups.
Used in Materials Science:
(4-nitrophenyl)(diphenyl)methanol is used as a component in the development of new materials, taking advantage of its chemical properties and potential interactions with other molecules.
Used as a Ligand in Coordination Chemistry:
(4-nitrophenyl)(diphenyl)methanol is used as a ligand to form coordination complexes with metal ions, which can have applications in catalysis, sensing, and other areas.
Used in Antimicrobial Agents Development:
(4-nitrophenyl)(diphenyl)methanol is used as a potential active ingredient in the development of new antimicrobial agents, given its demonstrated antibacterial and antifungal properties.

Upstream product

• 2945-12-2 1-(diphenylmethyl)-4-nitrobenzene 
• 71-43-2 benzene 
• 555-16-8 4-nitrobenzaldehdye 
• 63068-97-3 dichloro-(4-nitro-phenyl)-phenyl-methane 
• 74087-85-7 3,3-dimethyldioxirane 
• 62516-66-9 ((4-nitrophenoxy)methylene)dibenzene 
• 865-47-4 potassium tert-butylate 
• 75-65-0 tert-butyl alcohol 
• 41273-47-6 4-nitro-trityl chloride 

Downstream Products

• 95437-74-4 tert-butyl-(4-nitro-trityl)-peroxide 
• 128527-12-8 bis-[4-(α-hydroxy-benzhydryl)-phenyl]-diazene 
• 858784-45-9 N,N'-bis-[4-(α-hydroxy-benzhydryl)-phenyl]-hydrazine 
• 128527-13-9 bis-[4-(α-hydroxy-benzhydryl)-phenyl]-diazene-N-oxide 
• 857587-05-4 bis-[4-(α-chloro-benzhydryl)-phenyl]-diazene 
• 42365-21-9 bis-[4-(α-dehydro-benzhydryl)-phenyl]-diazene 
• 13189-74-7 4-nitro-trityl azide 

Relevant academic research and scientific papers

A three-aryl alcohol compound and its synthesis method

The invention discloses a three-aryl alcohol compound and its synthetic method, relates to the field of organic synthesis. The method is in the aerobic environment in a non-protic solvent, such as the formula (I) will be a compound represented by the gene

Oxidation of nitrobenzylic carbanions with dimethyldioxirane. New synthesis of quinomethanes and nitrobenzylic carbinols. First examples of methylation of carbanions with dimethyldioxirane

The reaction of nitrobenzylic carbanions with dimethyldioxirane (DMD) results in oxidation at the carbanion center or at the nitronate center to give nitrobenzylic carbinols or quinomethanes, respectively. Minor amounts of the methylation products are also formed. Both of these processes were observed for carbanions of (p-nitroaryl)diarylmethanes. The outcome of the oxidation process is very sensitive to the reaction conditions.

Electron Apportionment in Cleavage of Radical Anions. 1. Nitro-Substituted Benzyl Phenyl Ethers

The radical anions of 4-nitrobenzyl phenyl ethers undergo cleavage at least 10E4 times faster than the radical anions of corresponding 4-nitrophenyl benzyl ethers despite a perceived thermodynamic advantage for the latter set of reactions.It is suggested that this results reflects a kinetic advantage for cleavage reactions which take place with regioconservation of spin density.