767-63-5 Usage
Uses
Used in Pharmaceutical and Medical Research:
2,1,3-Benzoxadiazol-4-amine is utilized as a pharmaceutical intermediate for its demonstrated biological activities and potential therapeutic properties. Its presence in drug development is attributed to its ability to modulate various biological pathways, making it a candidate for the treatment of several diseases.
Used in Materials Science:
In the realm of materials science, 2,1,3-Benzoxadiazol-4-amine is employed as a key component in the development of organic semiconductors. Its unique structure allows it to contribute to the advancement of light-emitting materials for optoelectronic devices, showcasing its versatility beyond the medical field.
Used in Optoelectronic Devices:
2,1,3-Benzoxadiazol-4-amine is used as a component in the creation of light-emitting diodes (LEDs) and other optoelectronic devices due to its light-emitting properties. Its integration into these technologies is for enhancing performance and exploring new avenues in display and lighting solutions.
The multifaceted nature of 2,1,3-Benzoxadiazol-4-amine positions it as a valuable compound for continued research and development across different industries, with the potential to yield innovative solutions in medicine, materials science, and optoelectronics.
Check Digit Verification of cas no
The CAS Registry Mumber 767-63-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 767-63:
(5*7)+(4*6)+(3*7)+(2*6)+(1*3)=95
95 % 10 = 5
So 767-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H5N3O/c7-4-2-1-3-5-6(4)9-10-8-5/h1-3H,7H2
767-63-5Relevant academic research and scientific papers
Semmler-Wolff aromatization of 4-hydroxyimino-4,5,6,7-tetrahydro-[2,1,3] benzoxadiazole and 4-hydroxyimino-4,5,6,7-tetrahydro[2,1,3]benzoxadiazole 1-oxide and some properties of the obtained amines
Samsonov,Sal'Nikov,Volodarskii
experimental part, p. 868 - 878 (2011/07/08)
The Semmler-Wolff aromatization of 4-hydroxyimino-4,5,6,7-tetrahydro[2,1,3] benzoxadiazole and its 1-oxide derivative in sulfuric acid and in acetic anhydride gave 4-amino[2,1,3]benzoxadiazole and 4-acetamido[2,1,3]benzoxadiazole 1-oxide. Some reactions o
Semi-empirical PM3 calculations predict the fluorescence quantum yields (φ) of 4-monosubstituted benzofurazan compounds
Uchiyama, Seiichi,Santa, Tomofumi,Okiyama, Natsuko,Azuma, Kentaro,Imai, Kazuhiro
, p. 1199 - 1207 (2007/10/03)
We have elucidated the relationship between the fluorescence quantum yield (φ) of 4-monosubstituted benzofurazan (2,1,3-benzoxadiazole) compounds and the substituent group at the 4-position using a group of eleven such compounds. The absorption and fluore
