16483-98-0 Usage
Description
2,3-Diphenyl-2H-azirine is a nitrogen-containing heterocyclic compound with the molecular formula C14H12N. It is classified as an azirine, which is known for its high reactivity. 2,3-Diphenyl-2H-azirine has been studied for its potential use in organic synthesis and as an intermediate in the preparation of various compounds. Due to its reactivity, it is important to handle 2,3-Diphenyl-2H-azirine with care to avoid potential hazards.
Uses
Used in Organic Synthesis:
2,3-Diphenyl-2H-azirine is used as a reactive intermediate in organic synthesis for the preparation of various compounds. Its high reactivity allows for the formation of new chemical bonds and the synthesis of complex organic molecules.
Used in Chemical Research:
In the field of chemical research, 2,3-Diphenyl-2H-azirine is used to study the reactivity of aziridines and their potential applications in chemical reactions. Researchers investigate its behavior in different reaction conditions to understand its properties and explore new synthetic pathways.
Used in Pharmaceutical Industry:
2,3-Diphenyl-2H-azirine may be used as a building block or intermediate in the synthesis of pharmaceutical compounds. Its unique reactivity can be harnessed to create novel drug molecules with potential therapeutic applications.
Used in Material Science:
In material science, 2,3-Diphenyl-2H-azirine can be utilized in the development of new materials with specific properties. Its reactivity can contribute to the formation of polymers, coatings, or other materials with desired characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 16483-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,8 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16483-98:
(7*1)+(6*6)+(5*4)+(4*8)+(3*3)+(2*9)+(1*8)=130
130 % 10 = 0
So 16483-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H11N/c1-3-7-11(8-4-1)13-14(15-13)12-9-5-2-6-10-12/h1-10,13H
16483-98-0Relevant articles and documents
Visible-Light-Promoted [3 + 2] Cycloaddition of 2H-Azirines with Quinones: Access to Substituted Benzo[f]isoindole-4,9-diones
Wang, Lijia,Liu, Chuang,Li, Lei,Wang, Xin,Sun, Ran,Zhou, Ming-Dong,Wang, He
, p. 719 - 724 (2022/01/22)
A visible-light-promoteded [3 + 2] cycloaddition reaction of 2H-azirines with quinones has been developed under mild reaction conditions. The reaction provides a general and efficient strategy for the synthesis of the benzo[f]isoindole-4,9-diones scaffold
Harnessing in Situ Radical Oxygenation: Copper-Catalyzed Interrupted Azirine-Alkyne Ring-Expansion Reaction for the Synthesis of Pyrrolones
Sujatha, Chandragiri,Nallagangula, Madhu,Namitharan, Kayambu
supporting information, p. 4219 - 4223 (2021/06/21)
Here we report a novel interrupted azirine-alkyne ring-expansion reaction with molecular oxygen for the direct synthesis of highly functionalized pyrrolones enabled by copper catalysis. Mechanistic investigations indicate that the present three-component reaction proceeds via two copper-catalyzed sequential reactions, an azirine-ring-opening alkynylation and an amine-directed radical oxygenation, leading to the formation of interesting pyrrolone structures under mild conditions.
Photocatalytic Approach for Construction of 5,6-Dihydroimidazo[2,1- A[isoquinolines and Their Luminescent Properties
Wang, Zaibin,Li, Hanjie,Wang, Zhichao,Suleman, Muhammad,Wang, Yanguang,Lu, Ping
supporting information, p. 8101 - 8111 (2021/06/28)
A visible-light-driven photoredox reaction of tetrahydroisoquinoline with 2H-azirines is described. 4,7-Bis(4-methoxyphenyl)benzo[c][1,2,5]thiadiazole, a benzothiadiazole (BTD) derived fluorophore, is used as an organic photoredox catalyst, and the reacti
