62461-54-5 Usage
Uses
Used in Organic Synthesis:
2,6-Bis-(2-Thienyl)-4H-thiopyran-4-on is utilized as a building block in organic synthesis for the creation of a diverse array of organic molecules. Its structural attributes make it a valuable component in the synthesis of complex organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,6-Bis-(2-Thienyl)-4H-thiopyran-4-on is employed as a key intermediate in the development of new drugs. Its unique properties allow it to be a part of medicinal chemistry, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemicals:
2,6-Bis-(2-Thienyl)-4H-thiopyran-4-on also finds application in the agrochemical industry, where it may serve as a precursor to new pesticides or other agricultural chemicals, contributing to the development of more effective and environmentally friendly products.
Used in Materials Science:
Its potential use in materials science is attributed to the compound's electronic and optical properties, which make it a candidate for the development of new materials for electronic devices or sensors, thus expanding its utility in the realm of advanced materials.
Overall, 2,6-Bis-(2-Thienyl)-4H-thiopyran-4-on's versatility and the intriguing characteristics of its molecular structure position it as a promising compound for a wide range of applications, from organic synthesis to high-tech material development.
Check Digit Verification of cas no
The CAS Registry Mumber 62461-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,6 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62461-54:
(7*6)+(6*2)+(5*4)+(4*6)+(3*1)+(2*5)+(1*4)=115
115 % 10 = 5
So 62461-54-5 is a valid CAS Registry Number.
62461-54-5Relevant articles and documents
Chalcogenopyranones from disodium chalcogenide additions to 1,4- pentadiyn-3-ones. The role of enol ethers as intermediates
Leonard, Kristi,Nelen, Marina,Raghu, Madhavi,Detty, Michael R.
, p. 707 - 717 (2007/10/03)
Enol ethers 9 are formed as a mixture of E- and Z-isomers from the addition of ethanol to 1,4-pentadiyn-3-ones 2 in sodium ethoxide/ethanol. The enol ethers react with disodium chalcogenides to give the corresponding 2,6- disubstituted chalcogenopyranones
Synthesis of 2,6-Diaryl-4H-thiopyran-4-ones
Boaz, Neil W.,Fox, Kristine M.
, p. 3042 - 3045 (2007/10/02)
A novel synthesis of 2,6-diaryl-4H-thiopyran-4-ones has been developed.The title compounds were prepared by two sequential thio-Claisen condensations of a dialkyl ketone and two dithioesters.The intermediate β-thioxo ketone from the first condensation was converted to the corresponding β-(methylthio)enone for both protection and reactivity purposes.Facile addition-elimination of the methylthio moiety by a β-thioxo ketone enolate generated in the second thio-Claisen condensation afforded the desired heterocycle.This new method is rapid and simple with the only requirement being moderate substituent alkaline stability.
