63018-94-0 Usage
Uses
Used in Research and Development of Organic Light Emitting Diodes (OLEDs):
2,9,10-Trimethylanthracene is utilized as a chemical component in the research and development of organic light emitting diodes (OLEDs). Its unique electronic and optical properties contribute to the advancement of OLED technology, which has applications in various display and lighting systems.
Used in Production of Dyes and Pigments:
In the chemical industry, 2,9,10-trimethylanthracene is employed as a precursor in the synthesis of dyes and pigments. Its chemical structure allows for the creation of colorants with specific properties, such as color intensity and stability, which are valuable in various applications including textiles, plastics, and printing inks.
However, due to its potential environmental and health hazards, the use of 2,9,10-trimethylanthracene requires strict adherence to safety protocols and regulations. Careful handling and disposal are essential to minimize its impact on both human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 63018-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,1 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63018-94:
(7*6)+(6*3)+(5*0)+(4*1)+(3*8)+(2*9)+(1*4)=110
110 % 10 = 0
So 63018-94-0 is a valid CAS Registry Number.
63018-94-0Relevant academic research and scientific papers
Steric effects on [4+4]-photocycloaddition reactions between complementary anthracene derivatives
Bailey, David,Seifi, Nasim,Williams, Vance E.
, p. 313 - 318 (2011/09/16)
The steric effect of peripheral functional groups on the [4+4]-photocycloaddition between substituted anthracene derivatives was examined. The reactivity of 2,3,6,7-tetraphenylanthracene (TPA) with 2-phenylanthracene (PA), 2,9,10-trimethylanthracene (TMA) and 9,10-dimethyl-2,3-diphenylanthracene (DMDPA) was investigated. In all cases, the photodimers were formed in high yield despite the steric bulk of the peripheral substituents. It was further shown that although PA is capable of forming its homodimer, it selectively reacts with TPA when the latter is excited at 301 nm.
