3818-16-4 Usage
Description
1-(1,3-dioxo-2-phenyl-2,3-dihydro-1H-inden-2-yl)triaza-1,2-dien-2-ium is a complex chemical compound featuring a triaza-dien-ium group and a 1H-inden-2-yl moiety, interconnected by a dioxo-phenyl bridge. 1-(1,3-dioxo-2-phenyl-2,3-dihydro-1H-inden-2-yl)triaza-1,2-dien-2-ium holds potential in the realms of organic synthesis and medicinal chemistry, with possible applications in the creation of novel drugs and as a synthetic intermediate for other organic compounds. Further investigation is required to fully comprehend its properties and potential uses.
Uses
Used in Organic Synthesis:
1-(1,3-dioxo-2-phenyl-2,3-dihydro-1H-inden-2-yl)triaza-1,2-dien-2-ium is used as a synthetic intermediate for the development of various organic compounds. Its unique molecular structure allows for the creation of a wide range of chemical products, contributing to the advancement of organic chemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(1,3-dioxo-2-phenyl-2,3-dihydro-1H-inden-2-yl)triaza-1,2-dien-2-ium is used as a potential candidate for the development of new drugs. Its complex molecular structure may offer novel therapeutic properties, providing opportunities for the treatment of various medical conditions.
Used in Pharmaceutical Industry:
1-(1,3-dioxo-2-phenyl-2,3-dihydro-1H-inden-2-yl)triaza-1,2-dien-2-ium is used as a key component in the pharmaceutical industry for the synthesis of innovative drugs. Its unique properties and potential applications make it a valuable asset in the development of new medications to address unmet medical needs.
Used in Research and Development:
1-(1,3-dioxo-2-phenyl-2,3-dihydro-1H-inden-2-yl)triaza-1,2-dien-2-ium is also utilized in research and development settings, where scientists and chemists explore its properties, reactivity, and potential applications. The findings from these studies can lead to a better understanding of the compound's capabilities and its integration into various industries, including pharmaceuticals, materials science, and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 3818-16-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,1 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3818-16:
(6*3)+(5*8)+(4*1)+(3*8)+(2*1)+(1*6)=94
94 % 10 = 4
So 3818-16-4 is a valid CAS Registry Number.
3818-16-4Relevant articles and documents
Sulfonium ion-promoted traceless Schmidt reaction of alkyl azides
Ardiansah, Bayu,Kakiuchi, Kiyomi,Morimoto, Tsumoru,Tanimoto, Hiroki,Tomohiro, Takenori
supporting information, p. 8738 - 8741 (2021/09/08)
Schmidt reaction by sulfonium ions is described. General primary, secondary, and tertiary alkyl azides were converted to the corresponding carbonyl or imine compounds without any trace of the activators. This bond scission reaction through 1,2-migration of C-H and C-C bonds was accessible to the one-pot substitution reaction.
Ring Expansion of 2-Azido-2-phenyl-indan-1,3-dione for the Generation of Heterocyclic Scaffolds
Mittendorf, Fabia,Mohr, Fabian,Kirsch, Stefan F.
, p. 12760 - 12769 (2020/10/09)
A novel ring expansion based on the readily available 2-azido-2-phenyl-indan-1,3-dione is described. Treatment with primary amines and cesium carbonate in a two-step sequence gives rise to 3-amino-2,3-dihydroisoquinoline-1,4-diones with an unprecedented substitution pattern. The corresponding conversion using amino acid methyl esters leads directly to a novel tricyclic 1,10a-dihydroimidazo-isoquinoline-2,5,10-trione scaffold, a structure that has never been reported before, to the best of our knowledge.
