78914-77-9

Usage

Uses

Used in Chemistry:
[(E)-diazene-1,2-diyldibenzene-3,1-diyl]dimethanol is used as a chemical compound for its photochemical reaction capabilities and as a ligand in coordination chemistry due to its unique structure and properties.
Used in Organic Synthesis:
In the field of organic synthesis, [(E)-diazene-1,2-diyldibenzene-3,1-diyl]dimethanol is used as a building block for the synthesis of complex organic compounds, contributing to the development of novel materials and molecules.
Used in Material Science:
[(E)-diazene-1,2-diyldibenzene-3,1-diyl]dimethanol is utilized as a component in material science, where its properties can be harnessed to create or improve various materials for different applications.

Upstream product

• 619-25-0 3-Nitrobenzyl alcohol 
• 99-61-6 3-nitro-benzaldehyde 
• 60-29-7 diethyl ether 
• 168473-87-8 ethyl 4-bromo-3-nitrobenzoate 

Downstream Products

• 1877-77-6 3-aminobenzenemethanol 
• 175888-98-9 3,3'-hydrazodibenzenemethanol 
• 75125-65-4 bis<3-(chloromethyl)phenyl>diazene 
• 78914-78-0 Acetic acid 3-(3-acetoxymethyl-phenylazo)-benzyl ester 

Relevant academic research and scientific papers

A thermostable azo-linker for reversible photoregulation of DNA replication

Small molecules such as azobenzenes, one of the best reversible photo-switches, can be covalently incorporated into DNA to regulate its structures and functions with irradiation of the specific wavelengths. Using this strategy, a thermostable azobenzene l

Light-Controlled Regioselective Synthesis of Fullerene Bis-Adducts

Multi-functionalization and isomer-purity of fullerenes are crucial tasks for the development of their chemistry in various fields. In both current main approaches—tether-directed covalent functionalization and supramolecular masks—the control of regiosel

Azobenzene-Based Macrocyclic Arenes: Synthesis, Crystal Structures, and Light-Controlled Molecular Encapsulation and Release

Azobenzene (azo)-based macrocycles are highly fascinating in supramolecular chemistry because of their light-responsiveness. In this work, a series of azo-based macrocyclic arenes 1, 2, 3, and 4, distinguished by the substituted positions of azo groups, i

Palladium Nanoparticles on Silica Nanospheres for Switchable Reductive Coupling of Nitroarenes

Abstract: In this study, we synthesized a robust and sustainable Pd/SiO2 nanospheres catalyst. Further, its catalytic activity was demonstrated for the direct reductive coupling of nitroarenes under mild conditions. While the reaction with Pd nanoparticles on other supporting materials such as modified carbon materials and TiO2, under similar conditions, resulted formation of amines exclusively. Therefore, it was confirmed that the SiO2 was found to be the best supporting material towards the selective reductive coupling of nitroarenes. Also, the catalyst could be recycled up to five cycles with a marginal loss of product yield ( 2% yield). Graphic Abstract: [Figure not available: see fulltext.].