34824-20-9

Usage

Uses

Used in Organic Synthesis:
1,8-Bis(hydroxymethyl)anthracene is used as a building block in organic synthesis for the creation of various organic compounds. Its hydroxymethyl groups enable reactions that introduce further functionalization, making it a versatile component in the synthesis of complex organic molecules.
Used in Polymer Chemistry:
In polymer chemistry, 1,8-bis(hydroxymethyl)anthracene is used as a monomer or a cross-linking agent to produce polymers with specific properties. The hydroxymethyl groups can react with other monomers or polymers to form covalent bonds, contributing to the development of advanced polymeric materials.
Used in Materials Science:
1,8-Bis(hydroxymethyl)anthracene is utilized in materials science for the development of advanced materials with unique properties. Its fluorescent nature and potential for cross-linking make it suitable for applications in the creation of optical materials, sensors, and other specialized materials.
Used in Dye Development:
Due to its fluorescent properties, 1,8-bis(hydroxymethyl)anthracene is used as a precursor in the development of dyes for various applications, including textiles, inks, and other industries that require colorants with specific characteristics.
Used in Optical Materials:
1,8-BIS(HYDROXYMETHYL)ANTHRACENE's fluorescent properties make it useful in the development of optical materials, such as organic light-emitting diodes (OLEDs), fluorescent sensors, and other optoelectronic devices that require materials with specific light-emitting or light-absorbing properties.
Used in Research and Development:
1,8-Bis(hydroxymethyl)anthracene is employed in research and development for studying the properties of PAHs, their interactions with other molecules, and their potential applications in various fields. It serves as a model compound for understanding the behavior of similar compounds and developing new materials and applications based on their properties.

InChI:InChI=1/C16H14O2/c17-9-13-5-1-3-11-7-12-4-2-6-14(10-18)16(12)8-15(11)13/h1-8,17-18H,9-10H2

Upstream product

• 34824-75-4 1,8-diformylanthracene 
• 93655-34-6 dimethyl anthracene-1,8-dicarboxylate 
• 82-43-9 1,8-dichloroanthraquinone 
• 14381-66-9 1,8-dichloroanthracene 
• 92967-66-3 anthracene-1,8-dicarbonitrile 
• 158438-65-4 1-Formyl-8-hydroxymethylanthracen 
• 90866-50-5 1,8-dicyanoanthraquinone 
• 38366-38-0 9,10-dioxo-9,10-dihydroanthracene-1,8-dicarboxylic acid 
• 117-10-2 1,8-dihydroxy-9,10-anthracenedione 
• 64817-82-9 1,8-dihydroxy-9,10-dihydroanthracene 
• 38378-77-7 anthracene-1,8-dicarboxylic acid 

Downstream Products

• 158438-70-1 1-Hydroxymethyl-8-triphenylmethoxymethylanthracen 
• 34824-22-1 (8-Bromomethyl-anthracen-1-ylmethyl)-triphenyl-phosphonium; bromide 
• 34824-23-2 C₅₂H₄₂P₂⁽²⁺⁾*2Br^(1-) 

Relevant academic research and scientific papers

Solid-state esterification via ionic-to-covalent bond transformation in ionic molecular crystals consisting of disubstituted anthracene anion-cation combinations

Thermal solid-state reactions involving ionic-to-covalent bond transformation were achieved in the ionic molecular crystals of 1,8-bis[(pyridin-1-ium-1-yl)methyl]anthracene anthracene-1,8-dicarboxylate to produce the cyclic diester. The crystal structure given by X-ray diffraction analysis showed that the electrostatic interaction between the benzyl pyridinium cation and the carboxylate anion successfully works to locate these reaction sites close to each other and that there are channels for crystalline solvents and the liberated pyridine to escape. There by, the cyclic diester was selectively formed by the crystal-to-crystal reaction, which was proven by powder XRD profiles and optical microscopic and SEM images of the crystals before and after the reaction. This is the first thermal crystal-to-crystal condensation reaction. Another ionic molecular crystal of 1,8-bis[(pyridin-1-ium-1-yl)methyl]anthracene anthraquinone-1,8-dicarboxylate was also studied. There in, the corresponding cyclic diester was also obtained, but the crystals were transformed to amorphous solid by the reaction.

Fluorescent molecule for identifying mercury ions as well as preparation method and application

The invention discloses a fluorescent molecule for identifying mercury ions as well as a preparation method and application. Polycyclic aromatic hydrocarbons including a naphthalene ring or an anthracene ring and the like are used as starting raw materials and different identification sites are connected through a series of organic synthetic reaction (including substitution and addition) to obtainmolecular-tweezers-shaped main body compounds with different identification properties. The fluorescent molecule can be used for detecting the mercury ions and the problem that guest molecules cannotbe easily effectively identified through an existing molecule device is solved.

Synthesis of novel macrocyclic tetraamides

A simple and facile route has been described for the synthesis of macrocyclic tetraamides. This method is applicable for the preparation of a variety of macrocyclic tetraamides of various heteroatom substitutions.