36778-18-4

Usage

Uses

Used in Dye and Pigment Production:
1-(10-Methylanthracen-9-yl) is used as a key compound in the production of dyes and pigments for various applications, including the coloring of plastics, textiles, and inks. Its unique chemical structure contributes to the vibrant color properties and stability of the resulting dyes and pigments.
Used in Fluorescent Material Manufacturing:
1-(10-Methylanthracen-9-yl) is utilized as a component in the creation of fluorescent materials, which are essential in various industries such as biotechnology, medical imaging, and display technology. 1-(10-Methylanthracen-9-yl)'s ability to absorb and emit light makes it a valuable asset in these applications.
Used in Organic Electronic Devices:
1-(10-Methylanthracen-9-yl) is employed as a material in the development of organic light-emitting diodes (OLEDs) and organic photovoltaic cells. Its specific properties enhance the performance and efficiency of these devices, contributing to advancements in the field of organic electronics.
Used in Medicinal Chemistry:
1-(10-Methylanthracen-9-yl) has potential applications in medicinal chemistry, where its unique structure and reactivity can be harnessed for the development of new pharmaceuticals and therapeutic agents.
Used as a Precursor in Organic Synthesis:
1-(10-Methylanthracen-9-yl) serves as a precursor in the synthesis of other organic compounds, allowing for the creation of a diverse range of chemical products with various applications across different industries.

Upstream product

• 779-02-2 9-methylanthracene 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Relevant academic research and scientific papers

Polar Radicals. 16. Comments on a Recently Published Mechanistic Study of Photobromination Using Bromotrichloromethane

The mechanism of the photobromination reactions of a series of 10-substituted 9-methylanthracenes with bromotrichloromethane was reexamined.It was shown, contrary to the previous report, that the reaction proceeded by a mixed chain involving abstraction by both the bromine atom and the trichloromethyl radical.The kinetic results obtained from these reactions were shown to be dominated by reversible hydrogen transfer of the radicals formed in the reaction with the small amounts of hydrogen bromide produced from bromine atom abstraction.When the reactions were carried out in the presence of a hydrogen bromide scavenger, either ethylene oxide or powdered potassium carbonate, the kinetc results of photobromination were found to be almost insensitive to the effects of the changes in substituents.The reactivities of fluorene relative to the 10-substituted 9-methylanthracenes were found to be anomalously high, as was previously reported; however, when the reactions were carried out in the presence of ethylene oxide, the relative reactivities were shown to be predictably almost the same as those obtained when tert-butoxy radicals were the abstracting species.

Photobase generator

The object of the present invention is to provide a photobase generator capable of efficiently generating amines (tertiary amines and amidine) high in catalytic activity by sensing light with a wavelength of from 350 to 500 nm (especially, from 400 to 500 nm). The present invention is a photobase generator characterized in being represented by general formula (1) or (2). Y+ is a quaternary ammonio group of general formula (3) to (5), and X? is a counter anion selected from among a borate anion, a phenolate anion, and a carboxylate anion.