5839-61-2 Usage
Description
3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one is a complex organic compound with a unique molecular structure. It is characterized by its indole and pyrrole moieties, which are fused together to form a complex heterocyclic system. 3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one is of interest due to its potential applications in various fields, including pharmaceuticals, materials science, and chemical research.
Uses
Used in Pharmaceutical Applications:
3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one is used as a pharmaceutical compound for its potential therapeutic properties. 3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one's unique structure may allow it to interact with specific biological targets, such as receptors or enzymes, which could lead to the development of new drugs for various diseases.
Used in Materials Science:
In the field of materials science, 3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one may be used as a building block for the development of novel materials with specific properties. Its heterocyclic structure could be exploited to create materials with tailored electronic, optical, or mechanical properties for various applications, such as sensors, displays, or energy storage devices.
Used in Chemical Research:
3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one is also used as a research compound in the field of organic chemistry. Its synthesis and reactivity can provide valuable insights into the chemistry of complex heterocyclic systems, which could lead to the discovery of new synthetic methods or the development of new compounds with interesting properties.
Used in Application Industry:
3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one is used as an application type for a specific application reason. 3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one's unique properties and potential applications make it a valuable tool in this industry, where it can be utilized to achieve specific goals or solve particular challenges.
Note: The provided materials do not contain specific information about the uses of 3-[5-(1H-Indole-3-yl)-2,3-dihydro-2-oxo-1H-pyrrole-3-ylidene]-1H-indole-2(2H)-one. The uses listed above are hypothetical and based on the general properties and potential applications of complex organic compounds with similar structures.
Check Digit Verification of cas no
The CAS Registry Mumber 5839-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5839-61:
(6*5)+(5*8)+(4*3)+(3*9)+(2*6)+(1*1)=122
122 % 10 = 2
So 5839-61-2 is a valid CAS Registry Number.
5839-61-2Relevant articles and documents
Biosynthesis of Violacein: Evidence for the Intermediacy of 5-Hydroxy-L-tryptophan and the Structure of a New Pigment, Oxyviolacein, Produced by the Metabolism of 5-Hydroxytryptophan
Hoshino, Tsutomu,Ogasawara, Nagahiro
, p. 2339 - 2346 (2007/10/02)
The administration of 5-hydroxy-L-tryptophan to growing cells yielded a new blue pigment.The chemical structure was determined to be 5-(5-hydroxyindol-3-yl)-3-(5-hydroxy-3-oxoindolylidene)-4-pyrroline-2-one, mainly by using proton- and carbon 13-NMR.Feeding experiments of 5-hydroxytryptophan labeled with deuterium and carbon-13 unambiguously demonstrated that the hydroxylation of tryptophan was the first step for violacein biosynthesis.No incorporation of 5-hydroxy-tryptamine suggests that decarboxylation of 5-hydroxy-L-tryptophan was not the secondreaction, but should take place at a later stage in the pathway of violacein formation. 5-Hydroxy-indole was not incorporated, indicating that an enzyme like tryptophanase was unlikely to have been involved in violacein biosynthesis.
