28687-82-3 Usage
Description
[4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylis a complex organic compound characterized by a bioxazole ring and four phenyl groups attached to it. This unique molecular structure endows the compound with distinctive properties, making it a promising candidate for various applications in the fields of organic synthesis, materials science, optoelectronics, photochemistry, and pharmaceuticals.
Uses
Used in Organic Synthesis:
[4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylis used as a building block in organic synthesis for the creation of novel organic materials. Its unique structure allows for the development of new molecular architectures with potential applications in various industries.
Used in Materials Science:
In the field of materials science, [4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylis utilized for its potential in developing functional materials. [4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenyl-'s properties make it a valuable tool in designing materials with specific characteristics for use in different applications.
Used in Optoelectronics:
[4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylis used as a component in the development of optoelectronic devices. Its unique structure and properties contribute to the advancement of technology in this field.
Used in Photochemistry:
[4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylis also used in photochemistry, where its specific characteristics can be exploited to enhance the efficiency and performance of photochemical reactions.
Used in Pharmaceutical Industry:
[4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylis used as a component in novel drug development. Its unique structure may contribute to the creation of new pharmaceutical compounds with potential therapeutic applications.
Used in Organic Electronics:
In the field of organic electronics, [4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylis used for its potential in developing new electronic materials and devices, thanks to its specific properties and molecular structure.
Further research and exploration of [4,4'-Bioxazole]-5,5'(4H,4'H)-dione,2,2',4,4'-tetraphenylmay reveal even more potential uses for this versatile compound across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 28687-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,8 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28687-82:
(7*2)+(6*8)+(5*6)+(4*8)+(3*7)+(2*8)+(1*2)=163
163 % 10 = 3
So 28687-82-3 is a valid CAS Registry Number.
28687-82-3Relevant articles and documents
OXIDATION OF MESOIONIC OXAZOLONES BY OXYGEN
Rodriguez, H.,Marquez, A.,Chuaqui, C. A.,Gomez, B.
, p. 5681 - 5688 (2007/10/02)
The reaction of molecular oxygen with several 2,4-disubstituted oxazolones (3a-3g) is studied in the present paper.It is shown that oxygen may induce oxidative dimerization to dehydrodimers (7a-7g) via the mesoionic form of the oxazolone.The equilibration
GENERATION AND FATE OF FREE RADICALS OF Δ2-OXAZOLIN-5-ONES
Marquez, A.,Chuaqui, C. A.,Rodriguez, H.,Zagal, L.
, p. 2341 - 2346 (2007/10/02)
The reaction of Δ2-oxazolin-5-ones 1a and 1b with nickel peroxid in benzene produces the corresponding 4,4-dehydrodimers 5a and 5b as the main products in yields over 75percent.Under the same conditions, the 2-aryl-4-methyl-Δ2-oxazolin-5-ones 1c, 1d and 1e yield five products.In the case of 1c, the constituents of the product mixture were separated and identified as two 4,4-dehydrodimers (meso and dl pair isomers) 5c and 5c', (40.7percent), 2,4-dehydrodimer 6c (34.9percent), acetylanisoylimide 8c(8.5percent) and anisamide (15.9percent).Adequate mechanistic schemes are discussed to account for the products formed.
